BACITRACIN ZINC- bacitracin zinc ointment 
Family Dollar Services Inc.

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 Family Dollar 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 Allert:   •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 punture 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 reation 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? 1-800-432-8534 between 9 am and 4 pm EST, Monday–Friday.


Family wellness
NDC 55319-110-56
Bacitracin Zinc Ointment, USP
First Aid Antibiotic
Helps prevent 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:55319-110
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:55319-110-56 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 - Family Dollar Services Inc. (024472631)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 6/2017
Document Id: 6aba38ab-f1e0-4486-aaf4-7c2956703be5
Set id: e0f1b377-967d-4a8b-9b99-d248a6888c42
Version: 4
Effective Time: 20170619
Family Dollar Services Inc.