Label: TRIPLE ANTIBIOTIC CVS- bacitracin, neomycin, polymyxin ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 69842-047-02 - Packager: CVS
- 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 November 20, 2017
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
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WARNINGS
Warnings
For external use only. Do not use in the eyes, over large areas of the body. When using this product keep out of eyes. Rinse eyes with water to remove. Do not puncture or incinerate. Contents under pressure. Ask a doctor before use if you have condition or symptoms get worse or last more than one week, symptoms clear up and occur again within a few days.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC CVS
bacitracin, neomycin, polymyxin ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69842-047 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 500 U in 1 g BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 400 U in 1 g Inactive Ingredients Ingredient Name Strength Glycerin (UNII: PDC6A3C0OX) Mineral Oil (UNII: T5L8T28FGP) Pentylene Glycol (UNII: 50C1307PZG) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69842-047-02 56 g in 1 CAN; Type 0: Not a Combination Product 02/14/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 02/14/2014 Labeler - CVS (062312574)