DRMITSUI ECZEMA RELIEF- hydrocortisone 1% eczema relief cream

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Use

·Temporarily relieves the itching and discomfort associated with minor skin irritations, rashes, and inflammation, and due to eczema.
·Other uses of this product should only be under the advice and supervision of a doctor.

Warnings

For external use only

Do not use

For the treatment of diaper rash. Consult a doctor.

Stop Use

condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor

Ask Doctor

condition worsens, symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked 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: ask a doctor.

Other information

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

Inactive ingredients

Cetyl Alcohol, Glycerin, Avena sativa (oat) kernel extract, Bisabolol, Glyceryl stearate, Isohexadecane, Magnesium ascorbyl phosphate, Maltodextrin, Borneol, Menthol.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DRMITSUI ECZEMA RELIEF 
hydrocortisone 1% eczema relief cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-181
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
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
ISOHEXADECANE (UNII: 918X1OUF1E)
BORNEOL (UNII: M89NIB437X)
OAT (UNII: Z6J799EAJK)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
MENTHOL (UNII: L7T10EIP3A)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
BISABOLOL (UNII: 24WE03BX2T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-181-01	20 g in 1 TUBE; Type 0: Not a Combination Product	04/08/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/08/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd		411295811	manufacture(85248-181)