HEALMUSZ ECZEMA

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2024-01-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:12:52

Label at a glance#

ProductHEALMUSZ ECZEMA
Active ingredientHYDROCORTISONE
Label structure13 sections

Dosage and administration

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

Storage and handling

contents filled by weight, not volume

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrocortisone 1%

Purpose

OTC - PURPOSE SECTION

Anti-itch

Use

INDICATIONS & USAGE SECTION

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

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

or the treatment of diaper rash. Consult a doctor.

When Using

OTC - WHEN USING SECTION

avoid contact with eyes do not use more than directed unless told to do so by a doctor.

Stop Use

OTC - STOP USE SECTION

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

OTC - ASK DOCTOR SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

contents filled by weight, not volume

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-00684010-006-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1190aedd-74a7-c3c2-e063-6394a90a23070f97f777-588e-7655-e063-6394a90a2cfe2024-02-17WarningsExact identifier
spl set id: 0f97f777-588e-7655-e063-6394a90a2cfe

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.