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
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Drug Safety; save photos, receipts, labels, and correspondence before contacting the company.
- 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# 0005, within expiry
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
June 2, 2026
Reported by FDA DRUG
June 24, 2026
RecallRadar source check
June 30, 2026
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
Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000 units), net wt. 0.5 oz (14.2g), Product distributed by: Lil' Drug Store Products, Inc., 9300 Earhart Lane SW, Cedar Rapids, IA 52404, Made in India, UPC 3 66715 97310 8.. Reason: CGMP Deviations; deficiencies observed during FDA inspection. Classification: Class II. Quantity: 1225 tubes. Distribution: US Nationwide.
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Safety Guide
Not sure what to do next? Our guide walks you through the process step by step.
Read: How to Get Refunds and ReplacementsWant to Know First?
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