Label: TRIPLE ANTIBIOTIC ointment
- NDC Code(s): 58228-6209-1
- Packager: Front Line Safety
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 19, 2024
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
triple antibiotic ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58228-6209 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 [iU] in 1 g NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN 5 mg in 1 g POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B 5000 [iU] in 1 g Inactive Ingredients Ingredient Name Strength WHITE PETROLATUM (UNII: B6E5W8RQJ4) Product Characteristics Color Score Shape FREEFORM Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58228-6209-1 1800 in 1 CASE 01/26/2024 1 25 in 1 BOX 1 0.5 g in 1 PACKET; 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 01/26/2024 Labeler - Front Line Safety (061263699)