United States · FDA National Drug Code directory
Triple Antibiotic
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 51672-2120_534599e8-fece-b9dc-e063-6294a90ad09a
- Product NDC
- 51672-2120
- Form
- OINTMENT
- Composition / generic term
- Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20151215
- Source listing expiry
- 20271231
Source-listed ingredients
- BACITRACIN ZINC — 400 [iU]/g
- NEOMYCIN SULFATE — 3.5 mg/g
- POLYMYXIN B SULFATE — 5000 [iU]/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (51672-2120-1) / 14.2 g in 1 TUBE · 51672-2120-1
- 1 TUBE in 1 CARTON (51672-2120-2) / 28.4 g in 1 TUBE · 51672-2120-2
- 1 TUBE in 1 CARTON (51672-2120-3) / 60 g in 1 TUBE · 51672-2120-3
- 6 APPLICATOR in 1 CARTON (51672-2120-6) / .9 g in 1 APPLICATOR · 51672-2120-6
- 15 APPLICATOR in 1 CARTON (51672-2120-8) / .9 g in 1 APPLICATOR · 51672-2120-8
- 144 APPLICATOR in 1 CARTON (51672-2120-9) / .9 g in 1 APPLICATOR · 51672-2120-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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