Rapidol Triple Antibiotic Ointment Recall
Rapidol Triple Antibiotic First Aid Ointment in 2 oz (57 g) tubes has been recalled because FDA inspectors observed current good manufacturing practice deficiencies.
What matters now
- The affected product is Rapidol Triple Antibiotic First Aid Ointment in 2 oz (57 g) tubes.
- The product description lists three active ingredients and their strengths.
- FDA inspectors observed current good manufacturing practice deficiencies.
- Consumers should compare their ointment with the current FDA record and check that record for any next steps.
Product covered by the recall
The recall covers Rapidol Triple Antibiotic First Aid Ointment in 2 oz (57 g) tubes. The product is described as containing bacitracin zinc 400 units, neomycin sulfate 3.5 mg, and polymyxin-B sulfate 5,000 units.
Why the ointment was recalled
The FDA lists current good manufacturing practice deviations as the reason for the recall. The agency says deficiencies were observed during an FDA inspection.
What consumers should check
Compare the product name, tube size, active ingredients, and strengths with the current FDA record. Use the official record to confirm affected-product details and whether it lists any next steps before acting.
Action