Label: BACITRACIN- bacitracin zinc ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 52426-320-05, 52426-320-06 - Packager: Phoenix Global Supply Group, Inc
- 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 April 21, 2011
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- SPL UNCLASSIFIED SECTION
- Active ingredient (each gram contains)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredient
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- PRINCIPAL DISPLAY PANEL - 28.4 g Carton
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INGREDIENTS AND APPEARANCE
BACITRACIN
bacitracin zinc ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52426-320 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Bacitracin zinc (UNII: 89Y4M234ES) (Bacitracin zinc - UNII:89Y4M234ES) Bacitracin zinc 500 [iU] in 1 g Inactive Ingredients Ingredient Name Strength petrolatum (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52426-320-05 1 in 1 CARTON 1 14.2 g in 1 TUBE 2 NDC:52426-320-06 1 in 1 CARTON 2 28.4 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333B 04/01/2011 Labeler - Phoenix Global Supply Group, Inc (843189908)