FDA.reportPublic FDA data

HEALMUSZ Psoriasis

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:40:38

Label at a glance#

ProductHEALMUSZ Psoriasis
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

apply twice a day or as needed.

Storage and handling

store at room temperature.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 4% Dermatitis

Purpose

OTC - PURPOSE SECTION

Psoriasis and Seborrheic

Use

INDICATIONS & USAGE SECTION

relieves and helps prevent recurrence of: it ching irritation redness flaking scaling due to psoriasis and seborrheic dermatitis

Warnings

WARNINGS SECTION

For external use only.

When Using

OTC - WHEN USING SECTION

avoid contact with eyes.
If contact occurs, rinse thoroughly with water.

Stop Use

OTC - STOP USE SECTION

condition worsens or does not improve after regular use.

Ask Doctor

OTC - ASK DOCTOR SECTION

condition worsens or does not improve after regular use.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

apply twice a day or as needed.

Other information

STORAGE AND HANDLING SECTION

store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Borneol, Cetyl Alcohol, Dimethicone, Glyceryl 1-stearate, Menthol,Nifedipine, etc.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974603690392GTIN-13: 6974603690392
EAN-13: 6974603690392
GTIN storage (14 digits): 06974603690392		Label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
bbd94e90-e531-9113-45c1-29860f331640Product name720230104
5e4d0a9b-8ce4-418c-bf0c-d2b4be281ffdProduct name420220126
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
308fd2ea-d88a-e021-96c1-7c2ab74d6e4bProduct name120140508

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
84010-00784010-007-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
NIFEDIPINEI9ZF7L6G2LIACT
MENTHOLL7T10EIP3AIACT
BORNEOLM89NIB437XIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE92RU3N3Y1OIACT
GLYCERYL 1-STEARATE258491E1RZIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
4a4731a8-c7a4-68b8-e063-6394a90ae571118f51eb-82ce-5689-e063-6394a90acb4d2026-02-07WarningsExact identifier
spl set id: 118f51eb-82ce-5689-e063-6394a90acb4d

Reported adverse events (FAERS/openFDA)#

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