HYDROCORTISONE CREAM 1% cream

Hydrocortisone Cream 1% by

Drug Labeling and Warnings

Hydrocortisone Cream 1% by is a Otc medication manufactured, distributed, or labeled by Front Line Safety. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Hydrocortisone USP 1%

Purpose

Antipruritic (Anti-Itch)

Use(s)

For the Temporary relief of itching associated with minor skin irritations, inflammation, and rashes due to eczema, insect bites, poison ivy, poison oak, poison sumac, soaps, detergents, cosmetics, jewelry, seborrheic dermatitis, psoriasis, and for external genital, feminine, and anal itching

Warnings

For External Use Only

If pregnant or breastfeeding

Ask a health professional before use

Do not use

In the eyes For diaper rash For external genital or feminine itching if you have a vaginal discharge More than the recommended daily dosage unless directed by a doctor In the rectum by using fingers or any mechanical device or applicator

Stop use and ask a doctor if

Condition worsens or if symptoms persist for more than 7 days or clear up and occur again with a few days (do not continue to use this or any other hydrocortisone product for longer than 7 days)

Bleeding occurs due to anal itching

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) 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: Consult a doctor

When used for anal itching, cleanse the affected area with mild soap and warm water and rinse thoroughly. Gently dry, patting or blotting with bathroom tissue or soft cloth before applying.

Children under 12: Consult a doctor before using for anal itching.

Other Information

Store at room temperature 15º-30ºC (59º-86ºF) Avoid excessive heat Tamper Evident. Do not use if packet is torn, cut or opened.

Inactive Ingredients

Cetostearyl Alcohol, Glyceryl Monostearate SE, Methylchloroisothiazolinone, Propylene Glycol, Purified Water, Stearic Acid, Triethanolamine, White Petrolatum

Questions?

1-888-900-2920 Monday - Friday, 8AM - 4PM PST

Label

FL-2045

INGREDIENTS AND APPEARANCE

HYDROCORTISONE CREAM 1% 
hydrocortisone cream 1% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58228-6245
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
WATER (UNII: 059QF0KO0R)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
STEARIC ACID (UNII: 4ELV7Z65AP)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
TROLAMINE (UNII: 9O3K93S3TK)

Product Characteristics
Color		Score
Shape	FREEFORM	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58228-6245-1	1800 in 1 CASE	01/26/2024
1		25 in 1 BOX
1		0.9 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M032	01/26/2024

Labeler - Front Line Safety (061263699)