Label: TRIPLE ANTIBIOTIC PLUS MAXIMUM STRENGTH- bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 59450-823-56 - Packager: The Kroger Co.
- 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 March 20, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- OTC - ACTIVE INGREDIENT
- OTC - PURPOSE
- USES
- WARNINGS
- OTC - DO NOT USE
- OTC - ASK A DOCTOR BEFORE USE IF YOU HAVE
- OTC - WHEN USING THIS PRODUCT
- OTC - STOP USE AND ASK A DOCTOR IF
- OTC - KEEP OUT OF REACH OF CHILDREN
- 2 DOSAGE & ADMINISTRATION
- OTHER INFORMATION
- INACTIVE INGREDIENT
- OTC - QUESTIONS OR COMMENTS?
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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Kroger®
QUALITY GUARANTEED
Compare to the active ingredients of NEOSPORIN® PLUS.
*See Back Panel.
maximum strength
TRIPLE ANTIBIOTIC OINTMENT
PLUS PAIN RELIEF
• Bacitracin Zinc • Neomycin Sulfate • Polymyxin B Sulfate • Pramoxine Hydrochloride
• First aid antibiotic plus topical pain reliever
NET WT 1 OZ (28 g)
08230611xx VC108014
CARTON LABEL
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INGREDIENTS AND APPEARANCE
TRIPLE ANTIBIOTIC PLUS MAXIMUM STRENGTH
bacitracin zinc,neomycin sulfate, polymyxin b sulfate, pramoxine hcl ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59450-823 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59450-823-56 1 in 1 CARTON 1 28 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 07/01/2008 Labeler - The Kroger Co. (006999528)