- ACTIVE INGREDIENT
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Warnings:
For external use only
Dosage and Administration:
- •
- clean the affected areas
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- apply a small amount of product (an amount equal to the surface area of the tip of the finger) on the area 1 to 3 times daily
- •
- may be covered with a sterile bandage
Stop use and ask a doctor if
- •
- the condition persists or gets worse, or if a rash or other allergic reaction develops.
- Purpose
- Indications and Usage
- Other information
- Inactive ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BACITRACIN
bacitracin ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63187-299(NDC:67777-219) Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BACITRACIN (UNII: 58H6RWO52I) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN 500 [iU] in 1 g Inactive Ingredients Ingredient Name Strength MINERAL OIL (UNII: T5L8T28FGP) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63187-299-01 28.35 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 12/01/2009 Labeler - Proficient Rx LP (079196022) Establishment Name Address ID/FEI Business Operations Proficient Rx LP 079196022 REPACK(63187-299) , RELABEL(63187-299)