Label: TRIPLE ANTIBIOTIC- bacitracin zinc, neomycin, polymyxin b ointment
- NDC Code(s): 0363-0539-16, 0363-0539-26, 0363-0539-58, 0363-0539-64
- Packager: Walgreen Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 26, 2022
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- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- Use
- Warnings
- Directions
- Other information
- Inactive ingredient
- Questions or comments?
- SPL UNCLASSIFIED SECTION
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PRINCIPAL DISPLAY PANEL - 2 Tube Carton
TWIN PACK
NDC 0363-0539-26
Walgreens
Compare to the active ingredients in
Neosporin® Original Ointment††• WALLGREENS •
PHARMACIST RECOMMENDED†Triple
Antibiotic
OintmentBACITRACIN ZINC / NEOMYCIN SULFATE / POLYMYXIN B
SULFATE / FIRST AID ANTIBIOTICOriginal Strength
Triple Antibiotic- First aid antibiotic ointment
- Helps prevent infection in minor cuts, scrapes & burns
2
TUBES2 OZ (56 g) EACH, NET WT 4 OZ (112 g)
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
bacitracin zinc, neomycin, polymyxin b ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0539 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [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 5000 [USP'U] in 1 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) COCOA BUTTER (UNII: 512OYT1CRR) COTTONSEED OIL (UNII: H3E878020N) OLIVE OIL (UNII: 6UYK2W1W1E) SODIUM PYRUVATE (UNII: POD38AIF08) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 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:0363-0539-58 1 in 1 CARTON 08/26/2015 1 14 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:0363-0539-64 1 in 1 CARTON 05/07/2015 2 28 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:0363-0539-16 1 in 1 CARTON 08/29/2015 3 56 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:0363-0539-26 2 in 1 CARTON 11/24/2015 4 56 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 final part333B 05/07/2015 Labeler - Walgreen Company (008965063) Establishment Name Address ID/FEI Business Operations Natureplex LLC 062808196 MANUFACTURE(0363-0539)