VIADERMA CALM ANTI-ITCH- hydrocortisone solution

Viaderma Calm Anti-Itch by

Drug Labeling and Warnings

Viaderma Calm Anti-Itch 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

Hydrocortisone 1%

Purpose

Anti Itch

Uses

For the temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to:

eczema            detergents
insect bites      cosmetics
poison ivy        jewelry
poison oak        seborrheic dermatitis
poison sumac    psoriasis
soaps

Warnings

For external use only.

Avoid contact with the eyes
Do not use it for the treatment of diaper rash, consult a doctor

Keep out of reach of children.

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

Directions 

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: Do not use, consult a doctor.

Other information

• Store between 68-77°F (20-25°C)
• May stain cloth

Inactive ingredients

Acetic acid, caprylic/capric triglyceride, cholecalciferol, dimethyl sulfoxide, dipropylene glycol, gluconolactone, glycerin, histidine, hydroxyethyl-cellulose, magnesium stearate, sodium hydroxide, sorbic acid, stearic acid, tetrahexyldecyl ascorbate, tocopherol, water.

Package Labeling:

INGREDIENTS AND APPEARANCE

VIADERMA CALM ANTI-ITCH 
hydrocortisone solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71262-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
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)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
TOCOPHEROL (UNII: R0ZB2556P8)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71262-019-15	1 in 1 CARTON	11/14/2025
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	M006	11/14/2025

Labeler - VIADERMA DISTRIBUTION INC (081113521)

Registrant - VIADERMA DISTRIBUTION INC (081113521)