Home NDC 0713-0280 Bacitracin
Product NDC 0713-0280
11-digit product format 007130280
Labeler code 0713
Product ID 0713-0280_0cee4d1f-c118-adbd-e063-6294a90a74d8
Type HUMAN OTC DRUG
Nonproprietary name Bacitracin
Dosage form OINTMENT
Route TOPICAL
Labeler Cosette Pharmaceuticals, Inc.
Application M004
Marketing category OTC MONOGRAPH DRUG
Marketing start 1995-01-10
Substance BACITRACIN
Active strength 500 [USP'U]/g
Pharmacologic classes Decreased Cell Wall Synthesis & Repair [PE]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Bacitracin
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BACITRACIN 500 [USP'U]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 58H6RWO52I Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1648110 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0713-0280-31 Bacitracin 28.4 g in 1 TUBE OINTMENT 28.4 7
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Bacitracin ACTIVE INGREDIENT 58H6RWO52I BACITRACIN OINTMENT [PREFERRED PHARMACEUTICALS, INC] 2 Bacitracin ACTIVE MOIETY 58H6RWO52I BACITRACIN OINTMENT [PREFERRED PHARMACEUTICALS, INC] 2 Light Mineral Oil INACTIVE INGREDIENT N6K5787QVP BACITRACIN OINTMENT [PREFERRED PHARMACEUTICALS, INC] 2 Petrolatum INACTIVE INGREDIENT 4T6H12BN9U BACITRACIN OINTMENT [PREFERRED PHARMACEUTICALS, INC] 2 Bacitracin ACTIVE INGREDIENT 58H6RWO52I BACITRACIN (BACITRACIN) OINTMENT [G&W LABORATORIES, INC.] 1 Bacitracin ACTIVE MOIETY 58H6RWO52I BACITRACIN (BACITRACIN) OINTMENT [G&W LABORATORIES, INC.] 1 Light Mineral Oil INACTIVE INGREDIENT N6K5787QVP BACITRACIN (BACITRACIN) OINTMENT [G&W LABORATORIES, INC.] 1 Petrolatum INACTIVE INGREDIENT 4T6H12BN9U BACITRACIN (BACITRACIN) OINTMENT [G&W LABORATORIES, INC.] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0713-0280 BACITRACIN OINTMENT [COSETTE PHARMACEUTICALS, INC.] 7 Current NDC, Legacy NDC, 1 package rows 20231221_630e0841-baf2-e9fa-b309-ad1a5f95da3b.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 22 of 22 · 424 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Family Wellness Antiseptic and Pain Relief BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE FRONT PHARMACEUTICAL PLC cb7fdcde-2bd8-4834-ba4e-4d6fd1512599 2023-10-26 Warnings Exact identifier application number: M004 GENUINE FIRST AID Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. 23abfe12-5b50-4b49-878e-4fcdb6c341fd 2023-10-19 Warnings Exact identifier application number: M004 EVERLIT CARE Triple Antibiotic BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE Nantong Health & Beyond Hygienic Products Inc. f4921508-c32f-426f-a2f0-16c3acbd4713 2023-10-14 Warnings Exact identifier application number: M004 Cuadriderma BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE, AND PRAMOXINE HYDROCHLORIDE ProMex LLC 4fa99b96-ab4b-4523-82bc-343dbaf39fb6 2022-01-25 Warnings Exact identifier application number: M004
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0713-0280-31 00713028031 28.4 g in 1 TUBE (0713-0280-31) 28.4 g 1995-01-10 0000-00-00 No No Current