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Acid, dihydrate, sodium phosphate (Lenolax Paediatric)

Acid, dihydrate, sodium phosphate

Pharmacare limited û woodmead

Registration

Applicant
Pharmacare limited û woodmead
Registrations
1

Variants

ProductStrength and formRegistrationStatusScheduleLeaflets
Lenolax paediatric

EACH 1 ml SOLUTION CONTAINS ACID SODIUM PHOSPHATE, DIHYDRATE 160 mg SODIUM PHOSPHATE 60 mg

Not listedE1982E/11.5/1982RegisteredNot 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

  • S3: Sodium phosphate

    • in preparations intended for the management of faecal impaction or for bowel cleansing prior to surgical and diagnostic procedures. (S0)

    Consolidated Schedules 06 July 2026, lines 4251 to 4252

1 of 1 approved products with this ingredient carry S4 on their leaflet.

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.

Background

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Research articles

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