Lucky Super Soft Triple Antibiotic Ointment Recalled Over Manufacturing Concerns
An FDA recall record lists Lucky Super Soft First Aid Triple Antibiotic Ointment because of cGMP deviations and deficiencies observed during an FDA inspection. The product is described in 0.5-ounce (14-gram) tubes.
What matters now
- The affected product is Lucky Super Soft First Aid Triple Antibiotic Ointment.
- The ointment is listed in 0.5-ounce (14-gram) tubes.
- The recall reason is cGMP deviations and deficiencies observed during an FDA inspection.
- Check the exact product details against the current FDA record.
What product is involved
The recall record identifies Lucky Super Soft First Aid Triple Antibiotic Ointment in 0.5-ounce (14-gram) tubes. It lists dabur india limited as the brand.
How to identify the ointment
The product description lists bacitracin zinc 400 units, neomycin sulphate 3.5 mg, and polymyxin B sulphate 5,000 units. Parents and caregivers can use the product name, active ingredients, tube size, and listed brand to compare an ointment with the FDA record.
Why the product was recalled
The FDA record gives the reason as cGMP deviations and deficiencies observed during an FDA inspection.
What to check
Compare the ointment’s name, active ingredients, net weight, and listed brand with the current FDA recall record to confirm whether it matches the affected product.