AMERICAN RED CROSS ANTI-ITCH (hydrocortisone 1.0%- w/w spray

American Red Cross Anti-Itch by

Drug Labeling and Warnings

American Red Cross Anti-Itch by is a Otc medication manufactured, distributed, or labeled by Zhejiang Guoyao Jingyue Aerosol Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Hydrocortisone 1.0%(w/w)

Purpose

Anti-itch

Uses

• for the temporary relief of itching associated with minor skin irritation and rashes due to eczema,poison ivy, oak and sumac, cosmetics, soaps and detergents, jewelry, insect bites.
• Other uses of this product should be only under advice and supervision of a doctor.

Warnings

For external use only.

Flammable, keep away from heat, spark, electrical, fire or flame.

Do note use

Do nost use for the treatment of diaper rash. Consult a doctor.

When using this product

• avoid contact with eyes
• avoid contact with broken skin
• do not inhale or ingest. Use only as directed. Interntional misuse by deliberatebly concentrating and inhaling contents can be harmful or fatal.
• contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120 ºF.

Stop use and ask a doctor if

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again with a few days.

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 or older: apply to affected area not more than 3 to 4 times daily.
• children under 2 years of age: aks a doctor
• to apply to face, spray into palm of hand and gently apply.

Other information

• store cap tightly closed and at controlled room temperature
• harmful to wood finishes and plastics

Inactive ingredients

Water(Aqua)

Ethyl alcohol

Butane

Propane

Glycerin

Polyvinylpyrrolidone

Menthol

Label

INGREDIENTS AND APPEARANCE

AMERICAN RED CROSS ANTI-ITCH 
hydrocortisone 1.0%(w/w) spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75742-070
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PROPANE (UNII: T75W9911L6)
MENTHOL (UNII: L7T10EIP3A)
ALCOHOL (UNII: 3K9958V90M)
BUTANE (UNII: 6LV4FOR43R)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POVIDONE (UNII: FZ989GH94E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75742-070-01	141 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/22/2025

Labeler - Zhejiang Guoyao Jingyue Aerosol Co., Ltd. (554529812)

Establishment
Name	Address	ID/FEI	Business Operations
Zhejiang Guoyao Jingyue Aerosol Co., Ltd.		554529812	manufacture(75742-070)