POLY BACITRACIN- bacitracin zinc, polymyxin b sulfate ointment 
CVS Pharmacy

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.

----------

Poly Antibiotic Ointment - Bacitracin Zinc, Polymyxin B Sulfate

Drug Facts

Active ingredients (in each gram)

Bacitracin zinc, USP 500 units
Polymyxin B sulfate, USP 10,000 units

Purpose

First aid antibiotic

Uses

First aid to help prevent infection in

Warnings

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

Other information

Inactive ingredient

white petrolatum

Questions?

1-800-432-8534 between 9 am and 4 pm EST, Monday-Friday.

Principal Display Panel

CVS Health
Compare to the active ingredients in Polysporin®*
NDC 59779-003-56

Helps prevent infection
In minor cuts, scrapes & burns 

Poly Bacitracin
BACITRACIN ZINC - POLYMYXIN B SULFATE
First aid antibiotic ointment 

NET WT 1 OZ (28 g)

Poly Bacitracin
POLY BACITRACIN 
bacitracin zinc, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-003
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 [USP'U]  in 1 g
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B10000 [USP'U]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM (UNII: 4T6H12BN9U)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:59779-003-341 in 1 CARTON01/03/2005
114 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:59779-003-561 in 1 CARTON01/03/2005
228 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333B01/03/2005
Labeler - CVS Pharmacy (062312574)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

Revised: 11/2017
Document Id: e95e0e3e-b7f9-4f78-96a8-1dfeca319904
Set id: 7aa60cce-0860-43b6-bed1-dc3c07e55ad3
Version: 6
Effective Time: 20171116
 
CVS Pharmacy