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Oxybuprocaine (Minims Benoxinate Hydrochloride)

Oxybuprocaine

Soflens (Pty) Ltd

Registration

Applicant
Soflens (Pty) Ltd
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Minims benoxinate hydrochloride 0,4 %

EACH 100 ml CONTAINS OXYBUPROCAINE HYDROCHLORIDE 0,4 g

0,4 %C0044C/15.4/44RegisteredNot 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: Oxybuprocaine

    • when intended for ophthalmic or parenteral use;
    • except when contained in eye drops intended for the emergency treatment of “arc eyes”. (S2)

    Consolidated Schedules 06 July 2026, lines 7437 to 7441

  • S2: Oxybuprocaine

    • when contained in eye drops intended for emergency treatment of arc eyes.

    Consolidated Schedules 06 July 2026, line 2474

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.

C17H28N2O3308.40 g/mol

2-(Diethylamino)ethyl 4-amino-3-butoxybenzoate

Drag to rotate. Structure from PubChem CID 4633.

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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