FDA-Drug2026-06-24Class IIPROCESSING DEFECT

Rapidol Triple Antibiotic First Aid Ointment recalled for manufacturing deficiencies

OTHERNationwide distributionDrugs

What this means

The FDA found manufacturing deficiencies during an inspection of the facility that made Rapidol Triple Antibiotic First Aid Ointment. The product does not meet federal manufacturing standards. About 84 tubes (Lot 0004) were distributed nationwide.

  • Stop using this product if you have it.
  • Check your first aid supplies for Rapidol Triple Antibiotic ointment with UPC 8 10096 77162 9.
  • Dispose of affected tubes safely or contact Pharmadel LLC for return instructions.
  • Talk to a pharmacist or doctor if you have questions about an alternative antibiotic ointment.
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The agency's original wording
Hazard

CGMP Deviations; deficiencies observed during FDA inspection

Intended for
All ages
Illnesses reported
None reported
Sold states
US Nationwide.
Affected count
84 tubes
Manufactured in
225 - 4 - 1 Saily Village, Survey No, Dadra And Nagar Haveli, India
Products
Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5,000 units, net wt. 2oz (57g) tubes, Distributed by/por: Pharmadel LLC, New Castle, DE 19720, Made in India, UPC 8 10096 77162 9.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0633-2026

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