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SkinoRita Cream

NAFDAC Reg. No. A4-100358 · Drug

Registered with NAFDAC — registration activeAs of 6 November 2026 · synced automatically from official sources.
Product
SkinoRita Cream
NAFDAC number
A4-100358
Active ingredient
Urea; Latic acid; Glycine; Ammonium chloride; Sodium Chloride; Potassium chloride; Calcium lactate; Magnesium chloride; Sodium dihydrogen phosphate dihydrate; Stearic acid; Cetyl Alcohol; Glycerin; Disodium Edetate
Strength
see Composition
Form
Cream
Pack size
1 x 100 g (in HDPE jar)
Manufacturer
Not listed
Applicant (holder)
The Devon Pharmaceuticals Company Limited
Approved
28 Mar 2023
Status
Active View on NAFDAC ↗
Registration valid to
27 Mar 2028
WHO alerts
None found
Community reports
None
Times checked
0

RxVerify commentary

  • SkinoRita Cream is on the NAFDAC register with an active registration (A4-100358). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.

What SkinoRita Cream is used for

From the official U.S. FDA label for urea, the active ingredient registered with NAFDAC.

What it is used for

For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis pilaris, keratosis palmaris, keratoderma, corns and calluses, as well as damaged, ingrown and devitalized nails.

Possible side effects

Transient stinging, burning, itching or irritation may occur and normally disappear upon discontinuing the use of this product. To report SUSPECTED ADVERSE REACTIONS, contact Method Pharmaceuticals, LLC at 1-877-250-3427; or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .

Do not use if

Known hypersensitivity to any of the listed ingredients.

Warnings

For topical use only. Avoid contact with eyes, lips or mucous membranes.

General information only — not dosing advice. Always follow the leaflet in your pack and your doctor or pharmacist.

Check your pack of SkinoRita Cream

Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.

3 free checks left today · no signup Official sources: NAFDAC Green Book & recalls · WHO · U.S. FDA · NLM RxNorm

About SkinoRita Cream

What is in SkinoRita Cream?

SkinoRita Cream contains Urea; Latic acid; Glycine; Ammonium chloride; Sodium Chloride; Potassium chloride; Calcium lactate; Magnesium chloride; Sodium dihydrogen phosphate dihydrate; Stearic acid; Cetyl Alcohol; Glycerin; Disodium Edetate (see Composition), as cream, according to its NAFDAC registration record.

Is SkinoRita Cream registered with NAFDAC?

Yes. SkinoRita Cream is listed on the NAFDAC register under registration number A4-100358, and its registration is active as of 6 November 2026.

Has SkinoRita Cream been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches SkinoRita Cream in our automatically synced alert list.

How can I check that my pack of SkinoRita Cream is genuine?

Run a free authenticity scan with the NAFDAC number A4-100358, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

What is SkinoRita Cream used for?

For debridement and promotion of normal healing of hyperkeratotic surface lesions, particularly where healing is retarded by local infection, necrotic tissue, fibrinous or purulent debris or eschar. Urea is useful for the treatment of hyperkeratotic conditions such as dry, rough skin, dermatitis, psoriasis, xerosis, ichthyosis, eczema, keratosis pilaris, keratosis palmaris, keratoderma, corns and (Summarised from the official U.S. FDA label for urea. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.