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careone triple antibiotic

NDC 41520-679 · American Sales Company

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

41520-679-64 — 1 TUBE in 1 CARTON (41520-679-64) / 28 g in 1 TUBE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

41250-067 — bacitracin zinc, neomycin, polymyxin B, 41250-218 — Pramoxine HCl, Zinc acetate, 41250-433 — Bacitracin Zinc, Neomycin sulfate, Polymyxin B, Pramoxine HCl, 41250-679 — Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl, 41250-944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 41415-076 — Neomycin sulfate, Polymyxin B sulfate, and Pramoxine hydrochloride, 41415-120 — Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B, 41415-400 — Zinc Acetate and Pramoxine Hydrochloride, 41415-420 — Zinc Acetate and Pramoxine Hydrochloride, 41520-067 — bacitracin zinc, neomycin sulfate, polymyxin B sulfate, 42507-067 — bacitracin zinc, neomycin, polymyxin B, 42507-679 — Bacitracin, Neomycin, Polymyxin B, Pramoxine HCl, 42507-944 — glycerin, phenylephrine HCl, pramoxine HCl, white petrolatum, 42507-956 — Calamine Plus Spray, 42961-236 — bacitracin zinc, neomycin sulfate, polymyxin b sulfate, 43136-100 — BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HCl, 43473-012 — Bacitracin zinc, Neomycin sulfate, Polymyxin B sulfate, 43473-014 — Bacitracin zinc, Neomycin sulfate, Polymyxin B sulfate, 43473-016 — Bacitracin zinc, Neomycin sulfate, Polymyxin B sulfate, 43473-050 — Bacitracin zinc, Neomycin sulfate, 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.