Label: TRIPLE ANTIBIOTIC PLUS PAIN RELIEF- bacitracin, neomycin, polymyxin b, pramoxine hcl ointment
- NDC Code(s): 41250-679-16, 41250-679-58, 41250-679-64
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 23, 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
- •
- in the eyes
- •
- over large areas of the body
- Directions
- Other information
- Inactive ingredient
- Questions or comments?
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Principal Display Panel
MAXIMUM STRENGTH
triple antibiotic + pain relief ointment
Bacitracin Zinc | Neomycin Sulfate | Polymyxin B Sulfate | Pramoxine HCl
+ PAIN RELIEF
24 Hour Infection Protection
Soothes Cuts, Scrapes & Burns
Compare to Neosporin® + Pain Relief active ingredients
MAXIMUM STRENGTH
triple antibiotic + pain relief ointment
Bacitracin Zinc | Neomycin Sulfate | Polymyxin B Sulfate | Pramoxine HCl
+ PAIN RELIEF
NET WT 0.5 OZ (14 g)
First Aid Antibiotic/Pain Relieving Ointment
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC PLUS PAIN RELIEF
bacitracin, neomycin, polymyxin b, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-679 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 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) Product Characteristics Color WHITE (Translucent) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-679-58 1 in 1 CARTON 03/17/2010 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:41250-679-16 2 in 1 CARTON 03/17/2010 2 NDC:41250-679-64 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 03/17/2010 Labeler - Meijer Distribution Inc (006959555)