Active Ingredient
Bacitracin zinc 500 units
Bacitracin Ointment
FDA Label NDC 59898-720
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Water-jel Technologies for the product Bacitracin (NDC 59898-720). 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, keep out of the 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
- burns
Warnings
For external use only
Do Not Use
- in the eyes or 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
- a 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
Keep Out Of The 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 the 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 15 o to 25 oC (59 o to 77 o F)
- tamper evident sealed packets
- do not use any opened or torn packets
- you may report a serious adverse reaction to this product to 800-275-3433
Inactive Ingredient
petrolatum
Questions Or Comments?
1-800-276-3433 [email protected] www.waterjel.com
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