Label: BACITRACIN ZINC ointment
- NDC Code(s): 79503-107-30
- Packager: Ezricare Llc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 11, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use • in the eyes or apply over large areas of the body • if you are allergic to any of the ingredients • longer than 1 week unless directed by a doctor
Ask a doctor before use if you have deep or puncture wounds, animal bites, or serious burns
Stop use and ask a doctor if the condition persists or get worse, or if a rash or other allergic reaction develops
- Directions
- Other information
- Inactive ingredients:
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- Packaging
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INGREDIENTS AND APPEARANCE
BACITRACIN ZINC
bacitracin zinc ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79503-107 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) PARAFFIN (UNII: I9O0E3H2ZE) WHITE PETROLATUM (UNII: B6E5W8RQJ4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79503-107-30 1 in 1 CARTON 08/19/2021 07/01/2025 1 30 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 Drug M004 08/19/2021 07/01/2025 Labeler - Ezricare Llc (117573818)