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

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84010-006

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

1

HEALMUSZ ECZEMA 
salicylic acid 4% liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84010-006
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ) HYDROCORTISONE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
NIFEDIPINE (UNII: I9ZF7L6G2L)  
BORNEOL (UNII: M89NIB437X)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)  
MENTHOL (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84010-006-01100 g in 1 BOTTLE; Type 0: Not a Combination Product01/22/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00501/22/2024
Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
Establishment
NameAddressID/FEIBusiness Operations
Jiangxi Hemei Pharmaceutical Co., Ltd724892056label(84010-006) , manufacture(84010-006)

Revised: 1/2024
 
Jiangxi Hemei Pharmaceutical Co., Ltd