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Applied by Tanzania on the entire world
The measure came into effect on 07 May 2013
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 07 May 2013
- Publication where the measure is specified
- TZS 1597: 2013
- Regulation where the measure is specified
- TZS 1597: 2013 Caciotta cheese — Specification
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- This Tanzania Standard specifies requirements, methods of test and sampling for Caciotta cheese intended for direct consumption or for further processing
- Reference of the measure
- Clause 7
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Caciotta Cheese
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 03 July 2015
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 03 July 2015
- Publication where the measure is specified
- The Tanzania Food, Drugs and Cosmetics ACT, 2003
- Regulation where the measure is specified
- Tanzania, Food, Drugs and Cosmetics (Control of Medical Devices) Regulations, 2015
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 74.-(1) No person shall import or sell a medical device unless has a label that sets out the following information-
(a) the name of a medical device;
(b) the name and address of manufacturer;
(c) the identifier of a medical device, including the identifier of a medical device that is part of a system, test kit, medical device group, medical device family or medical device group family;
(d) batch or lot number;
(e) if the contents are not readily apparent, an indication of what the package contains, expressed in terms appropriate to a medical device, such as size, net weight, length, volume or number of units;
(f) the words “Sterile” if the manufacturer intends to sale a medical device in a sterile condition;
(g) the words “for single use only” if the medical device is intended for that purpose;
(h) the expiry date of the medical device expressed in month and year;
(i) unless self-evident to the intended user, the medical conditions, purposes and uses for which the medical device is manufactured, sold or represented, including the performance specifications of the medical devices if those specifications are necessary for proper use;
(j) the directions for use; and
(k) any special storage conditions applicable to the medical devices.
(2) The information required pursuant to subregulation (1) of this Regulation shall be expressed in a legible, permanent and prominent manner, in terms that are easily understood by the intended user.
(3) Subject to sub-regulation (4), if a medical devices is intended to be sold to the general public, the information required by sub-regulation (1) shall -
(a) be set out on the outside of the package that contains the medical devices; and
(b) be visible under normal conditions of sale. (4) Where a package that contains a medical devices is too small to display all the information in accordance with sub-regulation (1) of this Regulation, the directions for use shall accompany the medical device but need not be set out on the outside of the package or be visible under normal conditions of sale.
(5) Notwithstanding with provision of sub regulation (4) the accompany information shall be provided in the package inset, manual, booklet, or any other means as the case will be.
75. The information required by regulation 74 shall be in either English or Kiswahili or both English and Kiswahili. - Reference of the measure
- Part VIII Regulations 74 and 75
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Medical devices
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 31 July 2015
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 31 July 2015
- Publication where the measure is specified
- The Tanzania Food, Drugs and Cosmetics (Registration of Premises, Importation and Exportation of Pharmaceutical Products and Raw Materials) Regulations, 2015 GN. No. 312
- Regulation where the measure is specified
- Tanzania Food, Drugs and Cosmetics (Importation and Exportation of Pharmaceutical Products and Raw materials) Regulations, 2015.
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health and B: Protection of life and health of animals
- Description of the measure
- 22 (2) Subject to other conditions set in these Regulations, importation of free medical samples shall meet the following criteria: (a) samples shall bear a label printed “free sample – not for sale” in bold letters);
- Reference of the measure
- Part III Regulation 22(2) (a)
- Measure also domestic
- No
Products affected by the measure.
- Description
- Medical samples
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 31 July 2015
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 31 July 2015
- Publication where the measure is specified
- The Tanzania Food, Drugs and Cosmetics (Registration of Premises, Importation and Exportation of Pharmaceutical Products and Raw Materials) Regulations, 2015 GN. No. 312
- Regulation where the measure is specified
- Tanzania Food, Drugs and Cosmetics (Importation and Exportation of Pharmaceutical Products and Raw materials) Regulations, 2015.
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health and B: Protection of life and health of animals
- Description of the measure
- 26. Every importer shall ensure that all imported pharmaceutical products adhere to the following labeling requirements:-
(a) the information printed on labels are indelible, engraved or embossed on a primary and secondary container;
(b) the immediate outer packaging of the pharmaceutical products is clearly labeled in English or Swahili language or both;
(c) the trade or brand name where appropriate is stated;
(d) the international non-proprietary name (generic name) shall be clearly stated;
(e) quantities of active ingredients in the given formulation;
(f) date of manufacture and expiry;
(g) batch or lot number;
(h) storage conditions;
(i) name and address of manufacturer;
(j) registration number of the product issued by the authority in both outer and inner package of the product(s) where applicable;
(k) package insert literature must be in English or Kiswahili language;
(l) active pharmaceutical ingredient specification such as (BP, USP, JP, PhEur or PhInt). - Reference of the measure
- Part III Regulation 26
- Measure also domestic
- No
Products affected by the measure.
- Description
- Pharmaceutical products
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 05 August 2016
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 05 August 2016
- Publication where the measure is specified
- GOVERNMENT NOTICE NO. 229 ; THE WEIGHTS AND MEASURES ACT (CAP.340)
- Regulation where the measure is specified
- Weights and Measures (General) Regulations, 2016.
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 183. A producer or manufacturer of local goods or an importer, shall ensure that the goods are:
(b)if requiring labeling be labeled according to SADCMEL DOCUMENT 1 and OIML R 79 labeling requirements for pre- packed products as amended from time to time. - Reference of the measure
- Part XXII Regulation 183 (b)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- All products
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 30 January 2015
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 30 January 2015
- Publication where the measure is specified
- Industrial and Consumer ( Chemicals Management and Control ) Regulations Government Notice No. 25published on 30/1/2015
- Regulation where the measure is specified
- The Industrial and Consumer ( Chemicals Management and Control) Regulations , 2015
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health and E: Protection of the environment
- Description of the measure
- 4.-(1) An importer or exporter of chemicals shall, before importing or exporting a chemical-
(a) provide the Registrar with the details of the consignment;
(b) produce a corresponding invoice for importation;
(c) produce a purchasing order for exportation. - Reference of the measure
- Part II Regulation 4 (1)
- Measure also domestic
- No
Products affected by the measure.
- Description
- Chemicals
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 30 January 2015
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 30 January 2015
- Publication where the measure is specified
- Industrial and Consumer ( Chemicals Management and Control ) Regulations Government Notice No. 25published on 30/1/2015
- Regulation where the measure is specified
- The Industrial and Consumer ( Chemicals Management and Control) Regulations , 2015
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health and E: Protection of the environment
- Description of the measure
- 4(2) An importer or exporter of chemicals shall ensure that, all information and shipping documents and package are legible, in indelible print and be written in English or Kiswahili languages.
50. An importer, exporter, producer, distributor, seller, user or warehouse operator shall affix a label on the chemical to be imported, exported, transported, produced, distributed, sold , used or stored in the form and standard prescribed in the Nineteenth Schedule to these Regulations. - Reference of the measure
- Part II Regulation 4 (2);
Part XII Regulation 50 ; Nineteenth Schedule - ICC 10 - Measure also domestic
- Yes
Products affected by the measure.
- Description
- Chemicals
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Tanzania on the entire world
The measure came into effect on 05 April 2003
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 05 April 2003
- Publication where the measure is specified
- Industrial and Consumer ( Chemicals Management and Control ) Act , 2003
- Regulation where the measure is specified
- Industrial and Consumer Chemicals Short (Management and Control) Act, 2003,
- Country/Region applying the measure
- Tanzania
- Coded list of objectives
- A: Protection of human life and health and E: Protection of the environment
- Description of the measure
- 11 (5) Every chemical imported, distributed, manufactured, transported, sold, stored shall bear on the container thereof, a label with words ''Approved by the Board'', CAS and registration number, batch number and dates of manufacture, expiry, trade and chemical name, purity level of the substances and their identity or assay of percentage impurities, specification of active ingredient in terms of g/kg (grams per kilograms) or %, w/v (weight by volume), important physical chemical properties, Chemical Safety Cards, Material Safety Data Sheets where applicable instructions for appropriate storage compatibility and safety precautions.
42.-(I) Any person who produces, distributes, sells, transports, imports, exports, stores or deals in a chemical shall:-
(a) ensure the chemical is packaged according to recognized and approved national, international or foreign standards and the package shall bear a label as specified under sub-section (5) of section II of this Act; - Reference of the measure
- Part III Regulations 11(5) and 42 (1) (a)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Chemicals
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 22 September 1989
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 22 September 1989
- Publication where the measure is specified
- Control of Agricultural Chemicals Act CAP 29
- Regulation where the measure is specified
- Control of Agricultural Chemicals Act CAP 29
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 3 (1) No person shall import into or sell in Uganda any agricultural chemical unless that chemical has been registered, packed and labelled in accordance with regulations made under this Act and conforms to the standards specified in the regulations.
- Reference of the measure
- Regulation 3 (1)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Agricultural chemicals
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 28 March 2014
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 28 March 2014
- Publication where the measure is specified
- Statutory Instruments 2014, No. 34
- Regulation where the measure is specified
- The National Drug Policy And Authority (Importation And Exportation of Drugs) Regulations, 2014.
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 7 (1) The primary packaging of an imported drug shall be clearly labelled in English with the following—
(a) the trade or brand name, where appropriate;
(b) the generic name of the drug;
(c) the quantities of active ingredients in the drug;
(d) the dates of manufacture and expiry of the drug;
(e) the batch or lot number of the drug;
(f) any special conditions of storage applicable to the drug;
(g) the name and address of the manufacturer of the drug;
(h) a unique identification feature, if any; and
(i) the registration number of the drug, where applicable.
(2) The information leaflet enclosed in or accompanying the imported drug shall be in English.
(6) In subregulation (5), “evidence of alteration in the label” includes circumstances where—
(a) the entire label or a part of the label with the details such as the batch number or the date of manufacture of the
drug is removed;
(b) there is evidence of removal of the original label and evidence of attaching another label or evidence of placing a
label over the original label; or
(c) there is evidence of erasing or concealing the original details of the label and replacing the details with other
details.
15(3) The label on a primary container or package of the drug imported for donation shall be in English and where the original label on the primary container or package of the drug is not in English, the primary container or package of the drug shall bear an English translation which shall be permanently fixed to the container but which
shall not cover or erase the original label.
(4) The label referred to in sub regulation (3) shall bear—
(a) the name and address of the manufacturer of the drug;
(b) the generic name of the drug (INN);
(c) the date of manufacture of the drug and the batch or lot number of the drug;
(d) the date of expiry of the drug;
(e) the conditions under which the drug is to be stored; and
(f) the dosage, form and strength of the drug.
(5) The drug for donation shall be accompanied by the information of the prescriber of the drug, which shall be in English. - Reference of the measure
- Part II Regulation 7 (1);(2) and (6)
Part III Regulation 15 (3), (4) and (5) - Measure also domestic
- No
Products affected by the measure.
- Description
- Drugs
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 24 March 2014
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 24 March 2014
- Publication where the measure is specified
- Statutory Instruments 29 of 2014.
- Regulation where the measure is specified
- The National Drug Policy and Authority (Registration) Regulations, 2014.
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 29 (1) The applicant shall submit with the application for registration of a surgical instrument, a label which shall have—
(a) the name of the surgical instrument;
(b) the name and address of the manufacturer of the surgical instrument;
(c) the identifier of the surgical instrument, including the identifier of any surgical instrument or appliance that is part of a system, test kit or group;
(d) where the contents of the package of the surgical instrument are not readily apparent, an indication of what the package contains, expressed in terms appropriate to the surgical instrument, such as the size, net weight, length, volume or number of units;
(e) the word “Sterile”, if the manufacturer intends the device to be sold in a sterile condition;
(f) the expiry date of the surgical instrument, where applicable, to be determined by the manufacturer on the basis of the component of the surgical instrument, as the case may be, that has the shortest projected useful life;
(g) unless self-evident to the intended user, the medical conditions, purposes and uses for which the surgical instrument is manufactured, sold or represented, including the performance specifications of the surgical instrument, where those specifications are necessary for proper use;
(h) the directions for safe and effective use of the surgical instrument, unless directions are not required; and
(i) any special storage conditions applicable to the surgical instrument.
(2) The information required under subregulation (1) shall be provided in English, and shall be in a permanent and prominent manner, in terms that are easily understood by the intended user.
35 (2) Where the package that contains the surgical instrument or appliance is too small to display all the information required under regulation 29 on the outside of the package, the directions for the use of the surgical instrument or appliance shall accompany the surgical instrument or appliance. - Reference of the measure
- Part III Regulations 29 (1) & (2); Regulation 35 (2)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Surgical instruments
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 24 March 2014
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 24 March 2014
- Publication where the measure is specified
- Statutory Instruments 29 of 2014.
- Regulation where the measure is specified
- The National Drug Policy and Authority (Registration) Regulations, 2014.
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- A: Protection of human life and health
- Description of the measure
- 10 (1) The applicant shall at the time of applying for registration of a product provide a sample of the labelling and packaging for the product which shall contain—
(a) the brand name, where applicable;
(b) the international non-proprietary name or generic name of the product;
(c) the quantity of active ingredient per dosage unit;
(d) the pharmaceutical form and the quantity of active ingredient per dosage unit;
(e) the total contents of the primary, secondary and tertiary container;
(f) the date of manufacture of the product;
(g) the date of expiry of the product;
(h) the batch number of the product;
(i) the storage conditions;
(j) the product information for health professionals;
(k) the patient information and package leaflet; and
(l) the name and address of the manufacturer of the product. (2) The Authority shall not consider an application for registration of a product unless the words used in the labelling and packaging of the product are in English.
(3) The name and address of the manufacturer, the date of manufacture or the conditions of storage may be omitted from the primary packaging if the primary packaging is a blister, strip pack or a vial or an ampoule of less than ten millilitres.
(4) The name of the manufacturer may be substituted with a trade mark or other symbol associated with the manufacturer.
(5) Where the name and address of the manufacturer, the date of manufacture or the conditions of storage are omitted from the primary packaging under subregulation (3), they shall appear in full on the secondary packaging.
(7) The Authority shall only register a product with a clear, easily legible and comprehensible label. - Reference of the measure
- Part II Regulation 10(1),(2),(3), (4), (5) & (7)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Drugs
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 07 January 2005
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 07 January 2005
- Publication where the measure is specified
- Statutory Instruments Supplement to The Uganda Gazette No. 14 Volume XCVIII
- Regulation where the measure is specified
- Communications (Telecommunications and Radio Communications Equipment Type Approval) Regulations, 2005.
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- X: For purposes n.e.s.
- Description of the measure
- 7(14) Every importer or distributor shall ensure that any equipment offered for sale for local use is clearly labelled or affixed with—
(a) the trade name, model name and serial number;
(b) the manufacturer’s or supplier’s name; and
(c) a type approval label, approved by the Commission.
(15) An importer or distributor who is granted a type approval label by the Com mission, shall display the label in a conspicuous place.
(19) An apparatus shall have prominently displayed for a user—
(a) information on the intended use of the equipment and a declaration of its conformity to the applicable essential requirements; and
(b) sufficient information to identify the interfaces of telecommunications and radio communications networks to which the equipment is intended to be connected.
18(1) A manufacturer or importer of specified customer equipment or specified customer cabling shall apply on the equipment or cabling, a label that indicates that the equipment or cabling meets the prescribed standards. - Reference of the measure
- Regulation 7 (14), (15) and 19; Regulation 18(1)
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Telecommunications and radio communications
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Applied by Uganda on the entire world
The measure came into effect on 24 November 2011
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 24 November 2011
- Publication where the measure is specified
- Statutory Instruments No.4of 2012
- Regulation where the measure is specified
- Atomic Energy Regulations, 2012
- Country/Region applying the measure
- Uganda
- Coded list of objectives
- A: Protection of human life and health and E: Protection of the environment
- Description of the measure
- 98. Labeling requirements.
(1) Labeling shall be done in accordance with the assigned category for packages and overpacks.
(2) Packages and overpacks shall be assigned to either category IWHITE, II-YELLOW or III-YELLOW in accordance with the conditions specified in Figure 2, 3, 4 and 5, Schedule 7 and with the following requirements—
(a) for a package or overpack, both the transport index and the surface radiation level conditions shall be taken into account in determining which is the appropriate category;
(b) where the transport index satisfies the condition for one category but the surface radiation level satisfies the condition for a different category, the package or overpack shall be assigned to the higher category and category I-WHITE shall be regarded as the lowest category;
(c) the transport index shall be determined following the procedures specified in regulation 96.
(3) For all packages any labels which do not relate to the contents shall be removed or covered.
(4) Excepted packages shall not require any labeling.
(5) All other packages, overpacks and freight containers shall bear labels which conform to the models specified in Schedule 7.
(6) The labels referred to in this regulation shall be affixed to two opposite sides of the outside of a package or overpack or on the outside of all four sides of a freight container or tank.
(7) On large freight containers and tanks, enlarged labels may be used, in accordance with dimensions specified in Schedule 7, in which case no placarding shall be required.
99. Information required on labels. Labels shall be completed with the following information—
(a) contents—
(i) except for LSA-I material, the name(s) of the radionuclide(s) shall be as specified in Table 1, Schedule 11;
(ii) for mixtures of radionuclides, the most restrictive nuclides shall be listed to the extent the space on the line
permits;
(iii) the group of LSA or SCO shall be shown following the name(s) of the radionuclide(s) and the terms “LSA-II”,
“LSA-III”, “SCO-I” and “SCO-II” shall be used for this purpose; or
(iv) for LSA-I material, the term “LSA-I” is all that is required; the name of the radionuclide is not required;
(b) the maximum activity of the radioactive contents during transport expressed in units of Becquerel (Bq) with the
appropriate SI prefix;
(c) for overpacks and freight containers the “contents” and “activity” entries on the label shall bear the information
required in subregulations (a) and (b), respectively, totaled together for the entire contents of the overpack or freight
container except that on labels for overpacks or freight containers containing mixed loads of packages containing different radionuclides, such entries may read “See Transport Documents”;
(d) no transport index entry is required for category I-WHITE. - Reference of the measure
- Part XII Regulations 98 & 99
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Radioactive materials
Countries/Regions affected by the measure.
Inclusion/Exclusion Country Date in Date out Inclusion Entire world -
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 21 April 2015
- Publication where the measure is specified
- UGANDA GAZETTE Vol. CVIII No. 20 of 21 April 2015
- Regulation where the measure is specified
- US ISO 32:1977, Gas cylinders for medical use — Marking for identification of content
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard establishes a system of marking and a series of colours for the identification of the content of gas cylinders intended for medical use only.
- Reference of the measure
- US ISO 32:1977
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Gas cylinders
Countries/Regions affected by the measure.
-
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 21 April 2015
- Publication where the measure is specified
- UGANDA GAZETTE Vol. CVIII No. 20 of 21 April 2015
- Regulation where the measure is specified
- US ISO 7225:2005, Gas cylinders — Precautionary labels
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard specifies the design, content (that is, hazard symbols and text) and application of precautionary labels intended for use on individual gas cylinders containing single gases or gas mixtures. Labels for cylinders of bundles and labels for bundles are not covered by this standard..
- Reference of the measure
- US ISO 7225:2005
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- gas cylinders
Countries/Regions affected by the measure.
-
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 27 January 2014
- Publication where the measure is specified
- THE UGANDA GAZETTE Vol. CVII No. 5 of JANUARY 2014
- Regulation where the measure is specified
- US EAS 798:2013, Lipid food supplements – Requirements
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard specifies the requirements for lipid food supplements used for complementing the normal diet with essential fatty acids. This standard covers lipid food supplements primarily providing essential fatty acids and presented in forms such as capsules, paste or liquid. The product may be taken directly or added to another food with the primary objective of increasing the energy content of the food and provide essential fatty acids. This standard does not cover lipid food supplements intended for special dietary uses or medical/therapeutic purposes.
- Reference of the measure
- US EAS 798:2013
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- lipid food supplements
Countries/Regions affected by the measure.
-
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 27 January 2014
- Publication where the measure is specified
- THE UGANDA GAZETTE Vol. CVII No. 5 of JANUARY 2014
- Regulation where the measure is specified
- US EAS 346: 2013, Labelling of cosmetics — General requirements
- Country/Region applying the measure
- Uganda
- Description of the measure
- his Uganda Standard specifies requirements for the labelling of cosmetic products.
- Reference of the measure
- US EAS 346: 2013
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- cosmetic products
Countries/Regions affected by the measure.
-
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 25 October 2013
- Publication where the measure is specified
- Uganda Gazette Vol. CV No. 54 of 25th October 2013
- Regulation where the measure is specified
- US 1028:2013, Labelling requirements for prepackaged products (2nd Edition)
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard specifies requirements for the labelling of prepackaged products with constant nominal content with respect to the identity of the product, the name and place of business of the manufacturer, packer, distributor, importer or retailer and the net quantity of the product. This standard does not apply to the labeling of prepackaged foods for which a separate standard applies.
- Reference of the measure
- US 1028:2013
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- pre-packaged products
Countries/Regions affected by the measure.
-
Non-Tariff Measure
- NTM classification
- B31: Labelling requirements
- Date when the measure came into force
- 12 April 2013
- Publication where the measure is specified
- Uganda Gazette Vol. CV No. 17 of 12th April 2013
- Regulation where the measure is specified
- US 970-2:2012, Agglomerated stone-slabs and cut-to-size product — Part 2: Product requirements
- Country/Region applying the measure
- Uganda
- Description of the measure
- This Uganda Standard specifies labelling requirements for slabs and cut-to-size product of agglomerated stone which are made for use as vanity, kitchen tops and other similar uses in furnishing and modular tiles of agglomerated stone which are made for use as flooring and stairs for internal and external uses, fixed by mortar or adhesives.
- Reference of the measure
- US 970-2:2012,
- Measure also domestic
- Yes
Products affected by the measure.
- Description
- Agglomerated stone-slabs and cut-to-size product
Countries/Regions affected by the measure.
B31: Labelling requirements
