TETRACYTE FIRST AID AND ANTIBIOTIC TOPICAL- tetracycline hydrochloride ointment

Tetracyte First Aid and Antibiotic Topical by

Drug Labeling and Warnings

Tetracyte First Aid and Antibiotic Topical 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)

Tetracycline HCl 30 mg

Purpose

First aid antibiotic

Use

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, chlorhexidine gluconate, cholecalciferol, dimenthyl sulfoxide, dipropylene glycol, glucono delta lactone, glycerin, histidine, hydroxethyl-cellulose, magnesium stearate, methyparaben, sodium hydroxide, sorbic acid, water

Questions or comments?

Call 1-800-585-8685 or visit: www.viadermainc.com

Package Labeling:

INGREDIENTS AND APPEARANCE

TETRACYTE FIRST AID AND ANTIBIOTIC TOPICAL 
tetracycline hydrochloride ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71262-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TETRACYCLINE HYDROCHLORIDE (UNII: P6R62377KV) (TETRACYCLINE - UNII:F8VB5M810T)	TETRACYCLINE HYDROCHLORIDE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
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)
METHYLPARABEN (UNII: A2I8C7HI9T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
SORBIC ACID (UNII: X045WJ989B)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71262-011-01	1 in 1 CARTON	10/10/2024
1		15 g 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	10/10/2024

Labeler - VIADERMA DISTRIBUTION INC (081113521)