HEALMUSZ ECZEMA by Jiangxi Hemei Pharmaceutical Co., Ltd 84010-006下架

HEALMUSZ ECZEMA by

Drug Labeling and Warnings

HEALMUSZ ECZEMA by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

HEALMUSZ ECZEMA- salicylic acid 4% liquid 
Jiangxi Hemei Pharmaceutical Co., Ltd

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84010-006下架

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

or 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 Oot 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

HEALMUSZ ECZEMA 
salicylic acid 4% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-006
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
GLYCERIN (UNII: PDC6A3C0OX)
NIFEDIPINE (UNII: I9ZF7L6G2L)
BORNEOL (UNII: M89NIB437X)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
MENTHOL (UNII: L7T10EIP3A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-006-01	100 g in 1 BOTTLE; Type 0: Not a Combination Product	01/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/22/2024	02/17/2024

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	label(84010-006) , manufacture(84010-006)

Revised: 2/2024

Document Id: 1190aedd-74a7-c3c2-e063-6394a90a2307

34390-5

Set id: 0f97f777-588e-7655-e063-6394a90a2cfe

Version: 2

Effective Time: 20240217