Label: BACITRACIN ZINC ointment
- NDC Code(s): 0536-1263-28
- Packager: Rugby Laboratories
- 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 July 12, 2023
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- Active Ingredient
- Purpose
- Uses
- Warnings
- Do Not Use
- Ask Doctor before Use
- Stop Use and Ask Doctor if
- Directions
- Inactive Ingredients
- Questions
- Keep out of reach of children
- Other Information
- Packaging
-
INGREDIENTS AND APPEARANCE
BACITRACIN ZINC
bacitracin zinc ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0536-1263 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 MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) ALOE VERA LEAF (UNII: ZY81Z83H0X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0536-1263-28 1 in 1 BOX 04/15/2020 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 04/15/2020 Labeler - Rugby Laboratories (079246066) Registrant - Trifecta Pharmaceuticals USA LLC (079424163)