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Triple Antibiotic by Wal-Mart Stores, Inc.

Dosage form: ointment
Ingredients: BACITRACIN ZINC 400[USP'U] in 1g, NEOMYCIN SULFATE 3.5mg in 1g, POLYMYXIN B SULFATE 5000[USP'U] in 1g
Labeler: Wal-Mart Stores, Inc.
NDC Code: 49035-067

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.

Triple Antibiotic-bacitracin zinc, neomycin sulfate, and polymyxin b

Active Ingredient (in each gram)

Bacitracin zinc, USP 400 units
Neomycin sulfate, USP 3.5 mg
Polymyxin B sulfate, USP 5,000 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 (1-800-222-1222).


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 controlled room temperature 59°-86°F (15°-30°C)
• Protect from freezing
• Before using any medication, read all label directions. Keep carton, it contains important information.

Inactive ingredient

white petrolatum


Call: 1-888-287-1915

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NDC 49035-067-64
Compare to Neosporin® Active Ingredients
Triple Antibiotic
Bacitracin Zinc, Neomycin Sulfate and Polymyxin B Sulfate
First Aid Antibiotic Ointment
• Helps prevent infection

 NEW WT 1 OZ (28 g)

bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-067
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:49035-067-6428 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart333B08/31/2010
Labeler - Wal-Mart Stores, Inc. (051957769)

Revised: 05/2014
Wal-Mart Stores, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.