Active Ingredient
Bacitracin Zinc (500 units in each gram)
Bacitracin Zinc Ointment
FDA Label NDC 67777-008
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Bacitracin Zinc (NDC 67777-008). 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 active ingredient, purpose, uses, warnings, do not use, ask a doctor before use if you have, stop use and ask a doctor if, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
First Aid Antibiotic
Uses
First aid to help prevent infection in minor cuts, scrapes, and burns
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 gets worse, or if a rash or other allergic reaction develops
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
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 room temperature
- Avoid excessive heat and humidity
- Tamper Evident. Do not use if inner seal is torn, cut or opened.
Inactive Ingredients
Hard Paraffin, Liquid Paraffin, White Soft Paraffin
* Please review the disclaimer below.
