VIADERMA CARE FIRST AID ANTIBIOTIC- bacitracin zinc solution

Viaderma Care First Aid Antibiotic by

Drug Labeling and Warnings

Viaderma Care First Aid Antibiotic by is a Otc medication manufactured, distributed, or labeled by VIADERMA DISTRIBUTION INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each gram)

Bacitracin Zinc 500 units

Purpose

First aid antibiotic

Uses

• First aid to help prevent skin infection in minor cuts, scrapes, and burns

Warnings

For external use only.

Do not use

longer than 1 week unless directed by a doctor

in the eyes 

over large areas of the body

Ask a doctor before use if you have

deep or puncture wounds, animal bites, or serious burns.

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 

• clean the 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 between 68-77°F (20-25°C)
• may stain cloth

Inactive ingredients

Acetic acid, ascorbic acid, butylated hydroxyanisole, butylated hydroxytoluene, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, gluconolactone, glycerin, histidine, hydroxethyl-cellulose, magnesium stearate, sodium hydroxide, sorbic acid, water.

Package Labeling:

INGREDIENTS AND APPEARANCE

VIADERMA CARE FIRST AID ANTIBIOTIC 
bacitracin zinc solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71262-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BACITRACIN ZINC (UNII: 89Y4M234ES) (BACITRACIN - UNII:58H6RWO52I)	BACITRACIN	500 U  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71262-018-15	1 in 1 CARTON	12/05/2025
1		15 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M004	12/05/2025

Labeler - VIADERMA DISTRIBUTION INC (081113521)

Registrant - VIADERMA DISTRIBUTION INC (081113521)