HEALMUSZ ECZEMA- hydrocortisone 1% eczema 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.

When Using

■avoid contact with eyes
■do not use more than directed unless told to do so by 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

■contents filled by weight, not volume

Inactive ingredients

Borneol, Cetyl Alcohol, Glycerin, Glyceryl 1-Stearate, Menthol, Nifedipine, etc.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HEALMUSZ ECZEMA 
hydrocortisone 1% eczema cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-203
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
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
MENTHOL (UNII: L7T10EIP3A)
BORNEOL (UNII: M89NIB437X)
NIFEDIPINE (UNII: I9ZF7L6G2L)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-203-01	100 g in 1 TUBE; Type 0: Not a Combination Product	05/06/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/06/2026

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

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.		411295811	manufacture(85248-203)