Label: BACITRACIN ZINC ointment
- NDC Code(s): 49035-510-26
- Packager: EQUATE (Wal-Mart Stores, 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 November 20, 2019
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- Active ingredient (in each gram)
- Allergy alert:
- Do not use
- Ask a doctor before use if you have
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Other information
- Inactive ingredients
- Principal Display Panel
INGREDIENTS AND APPEARANCE
bacitracin zinc ointment
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-510 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 Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-510-26 1 in 1 CARTON 08/07/2017 1 28 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part333B 08/07/2017 Labeler - EQUATE (Wal-Mart Stores, Inc.) (051957769)