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Neomycin

NDC 67777-218 · Dynarex Corporation

Generic nameNeomycin Ointment
Dosage formOINTMENT
RouteTOPICAL
Active ingredient(s)NEOMYCIN SULFATE
Strength5 mg/g
Pharmacologic classAminoglycoside Antibacterial [EPC], Aminoglycosides [CS]
Marketing categoryOTC MONOGRAPH DRUG

Packages

67777-218-01 — 1000 BOX in 1 CASE (67777-218-01) / 10 PACKET in 1 BOX (67777-218-02) / .9 g in 1 PACKET

67777-218-03 — 1800 BOX in 1 CASE (67777-218-03) / 25 PACKET in 1 BOX (67777-218-04) / .9 g in 1 PACKET

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

66715-5405 — Triple Antibiotic, 66715-9531 — triple antibiotic ointment, 66715-9631 — Triple Antibiotic, 66758-070 — neomycin sulfate, polymyxin b sulfate and dexamethasone, 67091-272 — Bacitracin Zinc, Neomycin Sulfate, Poymyxin B Sulfate, and Pramoxine Hydrochrloride, 67091-274 — Bacitracin zinc, Neomycin sulfate, and Polymyxin B sulfate, 67234-031 — BACITRACIN ZINC, NEOMYCIN SULFATE, and POLYMYXIN B SULFATE, 67234-078 — bacitracin zinc, neomycin sulfate, polymyxin b sulfate, and pramoxine hydrochloride, 67234-081 — Bacitracin zinc, Neomycin sulfate, POLYMYXIN B SULFATE, and Pramoxine hydrochloride, 67777-217 — bacitracin zinc, neomycin sulfate and polymyxin b sulfate, 68001-483 — First Aid Antibiotic, 68016-296 — Premier Value Neomycin Sulfate, Polymyxin B Sulfate, Pramoxine HCL, 68016-319 — Bacitracin zinc, Neomycin Sulfate, Polymyxin B Sulfate, 68016-320 — Bacitracin zinc, Neomycin Sulfate, Polymyxin B Sulfate, 68016-715 — bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride, 68071-2211 — Polymyxin B Sulfate, Bacitracin Zinc and Neomycin Sulfate, 68071-2428 — Neomycin Sulfate, Polymyxin B Sulfate, and Dexamethasone, 68071-3359 — neomycin sulfate, polymyxin b sulfate and dexamethasone, 68071-4174 — Neomycin Sulfate, Polymyxin B Sulfate, Hydrocortisone, 68071-4229 — Neomycin sulfate, Polymyxin B Sulfate and Hydrocortisone, +327 more

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