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Triple Antibiotic and Burn Relief

NDC 69842-432 · CVS Pharmacy

Generic namebacitracin zinc, neomycin sulfate, polymyxin b sulfate, pramoxine hydrochloride
Dosage formOINTMENT
RouteTOPICAL
Active ingredient(s)BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE
Strength500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g
Pharmacologic classAminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

69842-432-58 — 1 TUBE in 1 CARTON (69842-432-58) / 14 g in 1 TUBE

69842-432-64 — 1 TUBE in 1 CARTON (69842-432-64) / 28 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69571-013 — Bacitracin Zinc, 69571-888 — Bacitracin zinc, Neomycin sulfate , Polymyxin B sulfate., 69729-615 — BACITRACIN, NEOMYCIN SULFATE, POLYMIXIN B SULFATE, PRAMOXINE HYDROCHLORIDE, 69729-616 — BACITRACIN, NEOMYCIN, POLYMYXIN B, PRAMOXINE, 69771-106 — Bacitracin Zinc, 69842-199 — bacitracin zinc, neomycin, polymyxin B, 69842-263 — Pramoxine HCL, 69842-265 — Pramoxine hydrochloride, menthol, 69842-400 — Pramoxine Hydrochloride and Zinc Acetate, 69842-420 — zinc oxide, 69842-562 — bacitracin, neomycin, polymyxin B, pramoxine hydrochloride, 69842-610 — Bacitracin, Neomycin, Polymyxin B, 69842-669 — Bacitracin Zinc, Neomycin sulfate, Polymyxin B, Pramoxine HCl, 69842-754 — neomycin, polymyxin B, pramoxine hydrochloride, 69918-515 — neomycin sulfate, polymyxin b sulfate and dexamethasone, 69968-0054 — Neomycin Sulfate, Polymyxin B Sulfate, and PRAMOXINE HYDROCHLORIDE, 69968-0055 — Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride, 69968-0056 — Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate, 69968-0057 — Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate, and Pramoxine Hydrochloride, 69968-0060 — Bacitracin Zinc and Polymyxin B Sulfate, +622 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels