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19. The name of the medicinal product.
20. The strength and pharmaceutical form of the product.
21. Where appropriate, whether the product is intended for babies, children or adults.
22. Where the product contains up to three active substances, the common name of each active substance.
23. The name of the holder of the marketing authorisation, Article 126a authorisation or traditional herbal registration relating to the product.
24. The product’s expiry date (month and year), in clear terms.
25. The manufacturer’s batch number.