BACITRACIN ZINC- bacitracin zinc ointment 
Kroger Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.


Bacitracin Zinc Oint USP Kroger part333B

Drug Facts

Active Ingredient (in each gram)

Bacitracin zinc, USP 500 units


First aid antibiotic


First aid to help prevent infection in   •minor cuts   •scrapes   •burns


For external use only

Allergy Alert:   •do not use if allergic to any of the ingredients

Do not use  •in the eyes  •over large areas of the body

Ask a doctor before use if you have  •deep or puncture wounds •animal bites  •serious burns

When using this product  •do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if  •condition persists or gets worse   •a 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.

Directions  •clean 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 59°-77°F (15°-25°C).   •Before using any medication, read all label directions.  Keep carton, it contains important information.

Inactive ingredient  white petrolatum

Questions? 1-800-632-6900



NDC 30142-501-56
Bacitracin Zinc Ointment, USP
First Aid Antibiotic  

Prevents Infection in Minor Cuts, Scrapes, and Burns. 

• Prevents Infection in Minor Cuts, Scrapes, and Burns. 

Net WT 1 OZ (28g)

Bacitracin Zinc Ointment
bacitracin zinc ointment
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-501
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Inactive Ingredients
Ingredient Name Strength
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:30142-501-56 1 in 1 CARTON 02/23/2012
1 28 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part333B 02/23/2012
Labeler - Kroger Company (006999528)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 12/2016
Document Id: de10ad33-22fb-4926-bf8c-1e9fbb66a0ff
Set id: 4cc980c9-3baa-4216-9c32-17ec5c8a4843
Version: 4
Effective Time: 20161212
Kroger Company