Label: TRIPLE ANTIBIOTIC ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 50607-5600-1, 50607-5600-2 - Packager: B8 Sales, Inc.
- Category: HUMAN OTC DRUG LABEL
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 April 2, 2010
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- SPL UNCLASSIFIED SECTION
- Drug Facts
- Active ingredients (in each gram)
- Purpose
- Uses
- Warnings
- Stop use and ask a doctor If
- Directions
- Other information
- Inactive ingredients
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC
triple antibiotic ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50607-5600 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Bacitracin Zinc (UNII: 89Y4M234ES) (Bacitracin Zinc - UNII:89Y4M234ES) Bacitracin Zinc 400 in 1 g Neomycin Sulfate (UNII: 057Y626693) (Neomycin - UNII:I16QD7X297) Neomycin Sulfate 5 mg in 1 g Polymyxin B Sulfate (UNII: 19371312D4) (Polymyxin B - UNII:J2VZ07J96K) Polymyxin B Sulfate 5000 in 1 g Inactive Ingredients Ingredient Name Strength petrolatum (UNII: 4T6H12BN9U) Product Characteristics Color white (white) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50607-5600-1 25 in 1 BOX 1 .9 g in 1 POUCH 2 NDC:50607-5600-2 144 in 1 BOX 2 .9 g in 1 POUCH Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333 05/01/2010 Labeler - B8 Sales, Inc. (833208635)