TRIASTEM TOPICAL ANTIBIOTIC- bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment 
ViaDerma Distribution, Inc.

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Triastem Topical Antibiotic Ointment

Drug Facts

Active Ingredient

Bacitracin Zinc 400mg in 1 g   Neomycin Sulfate 5 mg in 1 g  Polymyxin B Sulfate 5000 units in 1 g

Purpose

First Aid/Antibiotic

Indications

First aid to help prevent the risk of skin infection in minor cuts, scrapes, or burns.

Warnings

For external use only. May be harmful if swallowed.

Allergy Alert

Do not use if allergic to any ingredients in TriaStem™.

Do not use

  • in eyes
  • over large areas of the body
  • longer than 1 week unless directed by doctor

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious trauma

Stop use and ask a doctor

if condition persists or gets worse

Keep out of reach of children.

If swallowed, get medical help or contact a Poison control Center right away.

Directions

Stop use if product is misused

Other Information

Inactive Ingredients

acetic acid, ascorbic acid, chlorhexidine gluconate, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl-cellulose, magnesium stearate, sodium hydroxide, sorbic acid, stearic acid, water

Package Labeling:

Outer PackageInner PackageBottle

TRIASTEM TOPICAL ANTIBIOTIC 
bacitracin zinc, neomycin sulfate, polymyxin b sulfate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71262-005
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN400 mg  in 1 mL
NEOMYCIN SULFATE (UNII: 057Y626693) (NEOMYCIN - UNII:I16QD7X297) NEOMYCIN5 mg  in 1 mL
POLYMYXIN B SULFATE (UNII: 19371312D4) (POLYMYXIN B - UNII:J2VZ07J96K) POLYMYXIN B5000 U  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ACETIC ACID (UNII: Q40Q9N063P)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
GLUCONOLACTONE (UNII: WQ29KQ9POT)  
GLYCERIN (UNII: PDC6A3C0OX)  
HISTIDINE (UNII: 4QD397987E)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SORBIC ACID (UNII: X045WJ989B)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71262-005-151 in 1 BOX11/01/2019
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00411/01/2019
Labeler - ViaDerma Distribution, Inc. (081113521)

Revised: 12/2023
Document Id: 0b819764-5234-ae25-e063-6394a90ac73a
Set id: 133aed9d-44a1-4c7d-a00a-5072601e5a30
Version: 3
Effective Time: 20231202
 
ViaDerma Distribution, Inc.