Recall Weekly
Moderate riskFDA DrugClass II

Lucky Super Soft athlete's foot cream recalled for CGMP deviations

Dabur India Limited's Lucky Super Soft Antifungal Athlete's Foot Cream (Clotrimazole 1%, 1.5 oz tubes) is being recalled due to manufacturing deficiencies found during an FDA inspection. The affected lots (0001 and 0002) were distributed nationwide.

From the FDA notice · Read the official notice ↗

What to do

  1. Check if you have Lucky Super Soft Antifungal Athlete's Foot Cream with lot number 0001 or 0002.
  2. Stop using the product if you have an affected lot.
  3. Contact the manufacturer or your pharmacy for instructions on how to return or dispose of the product.
Official notice ↗

Is yours affected?

Compare your label or packaging with the recalled product.

Product
Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5.
UPC code
  • 808829104615
Sold in
Nationwide
Made for
Adults (0 months and older)

This recall covers 14 products — see all of them.

Details

Units affected
1102 tubes
Illnesses reported
None reported
Manufactured in
225 - 4 - 1 Saily Village, Survey No, Dadra And Nagar Haveli, India
Classification
Class II
Recall number
D-0629-2026

In the FDA's words

Description
Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for Delta Brands Inc., 580 White Plains Rd., Tarrytown, NY 10591 USA, Made in India, UPC 8 08829 10461 5. CGMP Deviations; deficiencies observed during FDA inspection Lot# 0001, 0002, within expiry Distribution: US Nationwide. Affected quantity: 1102 tubes
Hazard
CGMP Deviations; deficiencies observed during FDA inspection

14 products in this recall

Med Pride, Lucky and more creams recalled for quality issues

Dabur is recalling 14 antibiotic and antifungal creams, ointments and first aid products, including Lucky Super Soft, Circle K, Lil Drug Store, Rapidol, Cura Hongos and Med Pride. The FDA found manufacturing quality problems (CGMP deviations) during an inspection. No injuries have been reported.

The agency lists each product separately. Check every one you might have.

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