VITASTEM ULTRA- bacitracin zinc ointment 
ViaDerma Distribution, Inc

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Vitastem ULTRA

Drug Facts

Active Ingredient

Bacitracin Zinc (500 units Bacitracin in 1g)

Purpose

First Aid/Antibiotic

Uses

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 VitaStem™ ULTRA.

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 punture 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:71262-007-15

Outer Package2Inner Package2

Package Labeling:71262-007-55

Outer Package3Inner Package3

VITASTEM ULTRA 
bacitracin zinc ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71262-007
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I) BACITRACIN500 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)  
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
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:71262-007-151 in 1 CARTON06/01/2021
115 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:71262-007-551 in 1 CARTON06/01/2021
255 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00406/01/2021
Labeler - ViaDerma Distribution, Inc (081113521)

Revised: 12/2023
Document Id: 0b6df296-2efe-e3db-e063-6394a90a9653
Set id: fd96cc09-8522-44a5-b034-0d30e532410d
Version: 2
Effective Time: 20231201
 
ViaDerma Distribution, Inc