Neomycin, nitrofurazone, prednisolone, vitamin a palmitate (Prenine)
Neomycin, nitrofurazone, prednisolone, vitamin a palmitate
Elanco Animal Health (Pty) Ltd
Every registration of this product has been cancelled.
Registration
- Applicant
- Elanco Animal Health (Pty) Ltd
- Registrations
- 1
Variants
| Product | Strength and form | Registration | Status | Schedule | Leaflets |
|---|---|---|---|---|---|
| Prenine ointment EACH 100 g OINTMENT CONTAINS NEOMYCIN SULPHATE A 500 mgNITROFURAZONE A 250 mgPREDNISOLONE A 250 mgVITAMIN A PALMITATE A 125 mg | Ointment | 83/134 | Cancelled | Not determined | None |
Regulatory status
This product is still scheduled by law even when this site could not determine which tier it falls under. The label carries the S number in a square border; ask a pharmacist if you need to know its schedule.
Listings for this ingredient that could not be applied to this product
S4: Neomycin
- except when registered in terms of the provisions of the Fertilizers, Farm Feeds, Agricultural Remedies and Stock Remedies Act, 1947 (Act 36 of 1947).
Consolidated Schedules 06 July 2026, lines 7224 to 7225
S4: Nitrofurazone
- except when intended for application to the skin.
Consolidated Schedules 06 July 2026, line 7294
S4: Prednisolone
Consolidated Schedules 06 July 2026, line 7635
S2: Vitamin a
- and derivatives thereof and including retinol, retinal, retinoic acids and beta-carotene (but excluding isotretinoin) and not listed elsewhere in the Schedules, contained in preparations or mixtures containing more than 5 000 I.U (or 1 500 milligrams of the retinol equivalent or 3 000 milligrams of the beta-carotene equivalent) but not more than 10 000 I.U (or 3 000 milligrams of the retinol equivalent or 6 000 milligrams of the beta-carotene equivalent) of Vitamin A per recommended daily dose alone or in combination with other active pharmaceutical ingredients, except when registered in terms of the provisions of the Fertilizers, Farm Feeds, Agriculture Remedies and Stock Remedies Act, 1947 (Act 36 of 1947). (S0, S3)
Consolidated Schedules 06 July 2026, lines 2755 to 2761
S1: Nitrofurazone
- when intended for application to the skin.
Consolidated Schedules 06 July 2026, line 921
This is an informational summary of the Medicines and Related Substances Act 101 of 1965 and its 2017 General Regulations. It is not medical advice and not legal advice. Always check the medicine's label, which carries the schedule number inside a square border, or ask a pharmacist if you are unsure.
Combination product
This product contains more than one active ingredient, so it has no single molecular structure.
SAHPRA documents
SAHPRA has not published a professional information or patient information leaflet for this product.