Home NDC 80489-919 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF
Product NDC 80489-919
11-digit product format 804890919
Labeler code 80489
Product ID 80489-919_4928d0c5-0313-dfd6-e063-6394a90ab798
Type HUMAN OTC DRUG
Nonproprietary name bacitracin zinc, neomycin sulfate, polymyxin b sulfate
Dosage form OINTMENT
Route TOPICAL
Labeler OL PHARMA TECH, LLC Drs PHARMACY
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-09-05
Substance BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Active strength 500; 3.5; 10000; 10 [USP'U]/1000mg; mg/1000mg; [USP'U]/1000mg; mg/1000mg
Pharmacologic classes Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
NDC exclude flag No
Listing certified through 2027-12-31
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 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BACITRACIN ZINC 500 [USP'U]/1000mg NEOMYCIN SULFATE 3.5 mg/1000mg POLYMYXIN B SULFATE 10000 [USP'U]/1000mg PRAMOXINE HYDROCHLORIDE 10 mg/1000mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1359350 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 80489-919-01 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF 14000 mg in 1 TUBE OINTMENT 14000 1 80489-919-01 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF 1 in 1 CARTON OINTMENT 1 1 80489-919-02 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF 28300 mg in 1 TUBE OINTMENT 28300 1 80489-919-02 Drs. Pharmacy Triple Antibiotic AND BURN RELIEF 1 in 1 CARTON OINTMENT 1 1
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 48 of 115 · 2,286 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Freshnap Plus - 80% Ethyl Alcohol Towelette ALCOHOL TOWELETTE KARI-OUT LLC f4ae66e3-323b-5e2e-e053-2995a90acf42 2025-12-27 Warnings Exact identifier application number: M003 Guardelle BENZALKONIUM CHLORIDE Social Medical Supply LLC 8793e3be-7409-4f71-9397-abbeacd27cf8 2025-12-22 Warnings Exact identifier application number: M003 CareALL First Aid Burn Cream BENZALKONIUM CHLORIDE, LIDOCAINE HCL New World Imports, Inc 69eef888-0044-485c-96a1-247ed1204858 2025-12-22 Warnings Exact identifier application number: M003 Hand Sanitizer Pear Blossom Tea ALCOHOL SOLUTION Noshinku 46927edb-f8be-f0b9-e063-6294a90a8e56 2025-12-22 Warnings Exact identifier application number: M003 Hand Sanitizer Santal Blanc ALCOHOL SOLUTION Noshinku 4692c807-268e-6477-e063-6394a90aac0a 2025-12-22 Warnings Exact identifier application number: M003 Hand Sanitizer Vanilla Creme ALCOHOL SOLUTION Noshinku 4692e68c-2bc8-83f8-e063-6294a90a84e4 2025-12-22 Warnings Exact identifier application number: M003 Alcohol sanitizer wipes ALCOHOL/PURIFIED WATER SHANDONG HENGFA HYGIENIC PRODUCTS CO., LTD. ab9634bd-4226-2f73-e053-2995a90a802f 2025-12-19 Warnings Exact identifier application number: M003 Sanitizing Wipes BENZALKONIUM CHLORIDE Wipes LLC 9e9a76d9-23e0-4d3a-9903-8bf7aba54aa3 2025-12-19 Warnings Exact identifier application number: M003 Hand Sanitizer BENZALKONIUM CHLORIDE DGH Pharma, Inc. afeccd10-c7e5-6193-e053-2995a90a9a5a 2025-12-18 Warnings Exact identifier application number: M003 Hand Sanitizer BENZALKONIUM CHLORIDE DGH Pharma, Inc. ae4311f8-fc40-38a7-e053-2a95a90ae829 2025-12-18 Warnings Exact identifier application number: M003 Alcohol ALCOHOL Dynarex Corporation 88c5dcbe-185f-4966-b98b-25d50299e8df 2025-12-18 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE-IODINE TwinMed LLC fc8cb10c-4973-c0bd-e053-6394a90a6fdb 2025-12-18 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE-IODINE TwinMed LLC fcf27cbf-9535-1356-e053-6394a90a0362 2025-12-18 Warnings Exact identifier application number: M003 Povidone Iodine POVIDONE-IODINE TwinMed LLC fcf30b3a-c25b-7aaf-e053-6394a90affda 2025-12-18 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Black Raspberry ETHYL ALCOHOL 70% V/V Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 462ab5e8-029a-fe9d-e063-6294a90ac14d 2025-12-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Clementine Burst ETHYL ALCOHOL 70% V/V Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 462ad5ba-253f-2a30-e063-6294a90a261d 2025-12-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Honeydew Tart ETHYL ALCOHOL 70% V/V Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 462af072-6709-546f-e063-6294a90aacc8 2025-12-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Pear Blossom ETHYL ALCOHOL 70% V/V MY IMPORTS USA LLC 462b1d38-c7fa-992f-e063-6294a90ab78f 2025-12-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Black Raspberry ETHYL ALCOHOL 70% V/V MY IMPORTS USA LLC 462b2d3f-67b0-c393-e063-6294a90a208a 2025-12-17 Warnings Exact identifier application number: M003 AshleyBelle Moisturizing Hand Sanitizer Clementine Burst ETHYL ALCOHOL 70% V/V MY IMPORTS USA LLC 462b36d0-0a1f-bda8-e063-6294a90a5792 2025-12-17 Warnings Exact identifier application number: M003
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 80489-919-01 80489091901 1 TUBE in 1 CARTON (80489-919-01) / 14000 mg in 1 TUBE 1 tube 2021-09-05 No No Current 80489-919-02 80489091902 1 TUBE in 1 CARTON (80489-919-02) / 28300 mg in 1 TUBE 1 tube 2021-09-05 No No Current