FDA recall record

KENIL HEALTHCARE PRIVATE Optim V, Anti-Itch Cream, Benzocaine 20% & Resorcinol 3% - External recall — FDA D-0427-2025

CGMP Deviations

Class IIclassification
D-0427-2025official record ID
May 28, 2025report date

Recall record at a glance

Official recordD-0427-2025
CategoryDrug Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmKENIL HEALTHCARE PRIVATE LIMITED
Report dateMay 28, 2025
Recall initiation dateApr 24, 2025
Quantity6,372 Tubes
LocationTa. Kadi, District Mehsana, N/A, India

Official product description

Optim V, Anti-Itch Cream, Benzocaine 20% & Resorcinol 3% - External analgesic, Net Wt. Peso Neto 1 oz (28g) Tube, Distributed by: Pharmadel LLC, New Castle, DE 19720, Made in India, NDC 55758-300-01, UPC 8 59424 00420 6.

Why the product was recalled

CGMP Deviations

Distribution information

DE and NC

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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