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Table 2 Specific technical requirements in medicine legislation for countries which include requirements for outer packaging labelling [24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51].

From: Outer packaging labelling of medicines in Southern African Development Community (SADC) countries: comparative analysis of requirements and transition terms for harmonisation

Country

Medicines Legislation

Angola

None

Botswana

Information required for preservatives, ingredients such as paracetamol, aspirin and specific formulations, e.g., oral rehydration salts

Malawi

None

Mauritius

Requirement to include the following statement, “MOH & Wellness NOT FOR SALE”

Mozambique

None

Namibia

Information required for preservatives, ingredients such as paracetamol, tartrazine

South Africa

Requirements for barcode suitable for identification and tracking; South Africa is the only country that has provision for inclusion of regulatory information from other jurisdictions, i.e., manufacturer details and date, scheduling status and registration number allocated by other NMRAs

Seychelles

None

Tanzania

Special precautions for disposal of unused medicines or waste material from unused medicines, reimbursement conditions for social security, identification and authenticity, statement re government ownership of medicine

Zambia

None

Zimbabwe

Name and percentage of bacteriostatic or bactericidal agents