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TRIBIOTIC

Medically reviewed by Drugs.com. Last updated on Nov 9, 2021.

Dosage form: ointment
Ingredients: BACITRACIN ZINC 400[iU] in 1g, NEOMYCIN SULFATE 3.5mg in 1g, POLYMYXIN B SULFATE 5000[iU] in 1g
Labeler: HART Health
NDC Code: 50332-0032

TRIBIOTIC

Active Ingredients (in each gram)

Bacitracin Zinc 400 units

Neomycin Sulfate 5 mg (equivalent to 3.5mg neomycin base)

Polymyxin B Sulfate 5,000 units

Purpose:

Topical Antibiotic

Topical Antibiotic

Topical Antibiotic

Uses: First aid to help prevent infection and temporarily relieve pain in

  • minor cuts
  • scrapes
  • burns
  • abrasions

Warnings: For external use only

Serious burns require immediate medical attention


Allergy alert: Do not use if you are allergic to any of the ingredients

do not use

  • in or near the eyes
  • over large portions of the body
  • longer than 7 days unless directed by a doctor
  • more than 1 to 3 times daily

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

Stop use and ask a doctor if

  • condition worsens or lasts for more than 7 days
  • a rash or other allergic reaction occurs

Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Directions:

Do not use more than directed.

Adults and children 12 years of age and over:

  • clean the affected area
  • apply 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

Children under 12 years of age: ask a doctor

Petrolatum

TRIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50332-0032
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (BACITRACIN) BACITRACIN400 [iU]  in 1 g
NEOMYCIN SULFATE (NEOMYCIN) NEOMYCIN3.5 mg  in 1 g
POLYMYXIN B SULFATE (POLYMYXIN B) POLYMYXIN B5000 [iU]  in 1 g
Inactive Ingredients
Ingredient NameStrength
PETROLATUM 
Packaging
#Item CodePackage Description
1NDC:50332-0032-610 PACKET in 1 BOX, UNIT-DOSE
1.5 g in 1 PACKET
2NDC:50332-0032-325 PACKET in 1 BOX, UNIT-DOSE
2.5 g in 1 PACKET
3NDC:50332-0032-5144 PACKET in 1 BOX, UNIT-DOSE
3.5 g in 1 PACKET
4NDC:50332-0032-110 PACKET in 1 BOX, UNIT-DOSE
4.9 g in 1 PACKET
5NDC:50332-0032-225 PACKET in 1 BOX, UNIT-DOSE
5.9 g in 1 PACKET
6NDC:50332-0032-4144 PACKET in 1 BOX, UNIT-DOSE
6.9 g in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333B10/03/2005
Labeler - HART Health (069560969)

 
HART Health

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.