- Active ingredient (each gram contains)
- Purpose
- Uses
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Warnings
For external use only. This Unit Dose package is not child resistant and is intended for Institutional Use Only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Do not use
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- •in the eyes
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- •over large areas of the body
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- •if you are allergic to any of the ingredients
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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INGREDIENTS AND APPEARANCE
BACITRACIN
bacitracin ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55154-1950(NDC:45802-060) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 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:55154-1950-5 6 in 1 BAG 06/20/2011 1 0.9 g in 1 PACKET; 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 06/20/2011 Labeler - Cardinal Health (603638201)