HIGHFDA DRUG

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...

CGMP Deviations; deficiencies observed during FDA inspection

Source-backed recall notice

No product image was available from the source feed.

Official source
FDA DRUG
Recall date
June 2, 2026
Status
ACTIVE

Quick Facts at a Glance

Recall Date
June 2, 2026
Hazard Level
HIGH
Brand
Dabur India
Geographic Scope
1 states

What to Do Now

Use this page like a recall checklist: verify the product first, then act on the official remedy.

Immediate steps

  1. 1Stop using the product until you confirm whether it is included in the recall.
  2. 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
  3. 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
  4. 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.

Check these identifiers

Brand
Dabur India
Model numbers
Lot# 0001, 0002, within expiry
Where affected
ALL

Recall Timeline

Key dates and source checks for this recall record.

  1. Recall announced

    June 2, 2026

  2. Reported by FDA DRUG

    June 24, 2026

  3. RecallRadar source check

    June 30, 2026

  4. Consumer action

    Use the official remedy and keep documentation.

Hazard Information

CGMP Deviations; deficiencies observed during FDA inspection

What You Should Do

Consumers and healthcare providers should stop using this product immediately. Contact Dabur India Limited or your healthcare provider for guidance. Notification method: E-Mail

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Full 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.. Reason: CGMP Deviations; deficiencies observed during FDA inspection. Classification: Class II. Quantity: 1102 tubes. Distribution: US Nationwide.

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: How to Get Refunds and Replacements

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Product Classification

Product Details

Model Numbers
Lot# 0001
0002
within expiry
Affected States
ALL
Report Date
June 24, 2026
Source Agency
FDA - Drug Safety
Recall Status
ACTIVE

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