Bacitracin
Bacitracin is an FDA drug label for the active ingredient BACITRACIN manufactured by Cosette Pharmaceuticals, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231220.
Generic: BACITRACIN
Manufacturer: Cosette Pharmaceuticals, Inc.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 0713-0280
Application: M004
Effective: 20231220
Active Ingredients: ACTIVE INGREDIENT Bacitracin 500 units
Indications & Usage
USES first aid to help prevent infection in minor cuts, scrapes and burns
Dosage & Administration
DIRECTIONS • clean the affected area • apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily • may be covered with a sterile bandage
Contraindications
Not available.
Warnings
WARNINGS For external use only Do not use • if you are allergic to any of the ingredients • in the eyes • over large areas of the body • longer than 1 week unless directed by a doctor Ask a doctor before use in case of deep or puncture wounds, animal bites, or serious burns Stop use and ask a doctor if • the condition persists or gets worse • a rash or other allergic reaction develops
Adverse Reactions
Not available.
More from same ingredient
No related products.