Label: TRIPLE ANTIBIOTIC AND BURN RELIEF- bacitracin zinc, neomycin sulfate, polymyxin b sulfate, pramoxine hydrochloride ointment
- NDC Code(s): 69842-432-58, 69842-432-64
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2024
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- Official Label (Printer Friendly)
- Active ingredients (in each gram)
- Purpose
- Uses
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Warnings
For external use only
Do not use
- •
- if you are allergic to any of the ingredients
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- in the eyes
- •
- over large areas of the body
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
CVS Health®
Compare to the active ingredients in Neosporin® + Burn Relief
MAXIMUM STRENGTH± OINTMENT
Triple Antibiotic & Burn Relief
BACTIRACIN ZINC
NEOMYCIN SULFATE
POLYMYXIN B SULFATE
PRAMOXINE HCl
First aid antibiotic/pain relieving ointment
Infection protection and burn pain relief
BURN CARE
Package Contains One Tube
NET WT 0.5 OZ (14 g)
±Under OTC Monograph
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC AND BURN RELIEF
bacitracin zinc, neomycin sulfate, polymyxin b sulfate, pramoxine hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-432 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [USP'U] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN SULFATE 3.5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 10000 [USP'U] in 1 g PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE 10 mg in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-432-58 1 in 1 CARTON 03/05/2021 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:69842-432-64 1 in 1 CARTON 10/25/2022 2 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M004 03/05/2021 Labeler - CVS Pharmacy (062312574)