Label: BACITRACIN ZINC ointment
Contains inactivated NDC Code(s)
NDC Code(s): 67510-0055-1, 67510-0055-5
- Packager: Kareway Product, 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.
Updated July 16, 2012
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- Active ingredient (in each gram)
For external use only
Stop use and ask a doctor if
- you need to use longer than 1 week
- condition persists or gets worse
- rash or other allergic reaction develops
- Other information
- Inactive ingredients
- Package label
INGREDIENTS AND APPEARANCE
bacitracin zinc ointment
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67510-0055 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN ZINC 500 [USP'U] in 1 g Inactive Ingredients Ingredient Name Strength LIGHT MINERAL OIL (UNII: N6K5787QVP) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67510-0055-1 1 in 1 CARTON 1 28 g in 1 TUBE 2 NDC:67510-0055-5 1 in 1 CARTON 2 14 g in 1 TUBE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 07/24/2012 Labeler - Kareway Product, Inc. (121840057)