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Minoxidil (Regaine)

Minoxidil

Johnson & Johnson (Pty) Ltd û East London

Every registration of this product has been cancelled.

Registration

Applicant
Johnson & Johnson (Pty) Ltd û East London
Registrations
2

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Regaine

EACH 1 ml SOLUTION CONTAINS MINOXIDIL 20 mg

Not listedU0140U/13.4.2/140CancelledNot determinedNone
Regaine gel

EACH 1,0 g GEL CONTAINS MINOXIDIL 20,0 mg

GelY0031Y/13.4.2/31CancelledNot determinedNone

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: Minoxidil

    • exept when intended for application to the scalp in preparations containing not more than 2 percent (m/v) and which are registered in terms of the Act. (S2)

    Consolidated Schedules 06 July 2026, lines 7148 to 7149

  • S2: Minoxidil

    • when intended for application to the scalp in preparations containing not more than 2 percent (m/v) and which are registered in terms of the Act. (S4)

    Consolidated Schedules 06 July 2026, lines 2350 to 2351

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.

C9H15N5O209.25 g/mol

3-Hydroxy-2-imino-6-piperidin-1-ylpyrimidin-4-amine

Drag to rotate. Structure from PubChem CID 4201.

SAHPRA documents

SAHPRA has not published a professional information or patient information leaflet for this product.

Background

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Research articles

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