Drug Facts
-
Bacitracin Ointment
FDA Label NDC 41226-880
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kroger for the product Bacitracin (NDC 41226-880). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredients (each gram contains), purpose, uses, warnings, do no use, ask a doctor before use if you have, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients (Each Gram Contains)
Bacitracin 500 units
Purpose
First aid antibiotic
Uses
first aid to help prevent infection in:
- minor cuts
- scrapes
- burns
Warnings
For external use only.
Do No Use
- in the eyes
- over large areas of the body
- if you are allergic to any of the ingredients
Ask A Doctor Before Use If You Have
- deep or puncture wounds
- animal bites
- serious burns
Stop Use And Ask A Doctor If
- you need to use longer than 1 week
- condition persists or gets worse
- rash or other allergic reaction develops
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).
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
Other Information
- store at 20°-25°C (68°-77°F)
Inactive Ingredients
light mineral oil, white petrolatum
Questions Or Comments?
Call 1-800-632-6900
Package Label.Principal Display Panel
Bacitracin-label (Bacitracin Label)
Bacitracin-ifc (Bacitracin Ifc)
* Please review the disclaimer below.
