CLASS II ONGOING Drug recall · Reported 24 Jun 2026 · FDA Enforcement Report
Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc recalled
Dabur India is recalling Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc, Neomycin Sulfate 5 mg), distributed nationwide in the US. The recall was initiated on 2 Jun 2026 and the FDA has classified it as Class II.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0632-2026
- FDA event ID
- 99137
- Recalling firm
- Dabur India, Dadra And Nagar Haveli
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 2 Jun 2026
- FDA classified
- 26 Jun 2026
- Reported
- 24 Jun 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Manufacturing (CGMP) Deviations
- Drug class
- Creams, Ointments & Gels
Timeline
| 2 Jun 2026 | Recall initiated by company | |
| 24 Jun 2026 | Published in enforcement report | +22 days |
| 26 Jun 2026 | Classified by FDA | +2 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
CGMP Deviations; deficiencies observed during FDA inspection
Product as listed by the FDA
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.
Where it was distributed
US Nationwide.
Questions about this recall
Is Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc, Neomycin Sulfate 5 mg) recalled?
Yes. Dabur India recalled Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc, Neomycin Sulfate 5 mg) on 2 Jun 2026. The recall is Class II and its status is Ongoing. Recall number D-0632-2026.
Why was it recalled?
CGMP Deviations; deficiencies observed during FDA inspection
Which lots are affected?
Lot# 0005, within expiry
Where was it sold?
US Nationwide.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Dabur India
All 14| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS II | Med Pride, Bacitracin Zinc Ointment packets recalled by Dabur India | Dabur India | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Cura Hongos, Crema Antifungica, Clotrimazole 1% tubes recalled | Dabur India | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Circle K, triple antibiotic ointment, Bacitracin Zinc recalled | Dabur India | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc recalled | Dabur India | Manufacturing (CGMP) Deviations | Nationwide |
| Drug | CLASS II | Med Pride, 1% Clotrimazole Antifungal Cream recalled by Dabur India | Dabur India | Manufacturing (CGMP) Deviations | Nationwide |