Dabur India Limited — Rapidol recall — Check your batch

Home › Medicine › Dabur India Limited

Dabur India Limited

Check your batch

Check the batch codes below. If yours matches, return it for a refund rather than take it.

Class II

May cause temporary or medically reversible harm. Serious consequences are unlikely.
Refunds don't require a receipt, and you don't need proof of purchase.
FDA status: Ongoing.

What was recalled

Source: FDA · synced 29 Jul 2026 13:14

Check your batch Filed 2026-06-24

CGMP Deviations; deficiencies observed during FDA inspection

Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.

Check these codes: Lot# 0004, within expiry

84 tubes · distributed us nationwide. Recall D-0633-2026 on FDA.gov ↗

Watch Dabur India Limited for new recalls

One email per recall. Nothing else, ever.