CURITHYS

Manufacturer
J World
Effective date
2021-12-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:45:22

Label at a glance#

ProductCURITHYS
Active ingredientHYALURONATE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium hyaluronate

INACTIVE INGREDIENT SECTION

Niacinamide
Salicylic Acid
Sh-Oligopepide-1
Sh-Polypepide-1
TetraPeptide-44
Centella Asiatica Extract
Tranexamic acid
Camellia Japonica Flower Extract

OTC - PURPOSE SECTION

Micro-pyramid stimulates the skin and gives moisture and nutrition to sensitive skin.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Remove the protective film from the patch.

Attach it vertically to the desired site.

Re-press on thea ttached patch every few minutes..

Remove the patch after attaching for more than 1 hour.

WARNINGS SECTION

Use it for your own use only.

For external use only.

Discontinue use if adverse reaction occurs.

Contact a physician if symptoms persist.

Store at room temperature

.Do not reuse it as a disposable product.

Please use it immediately after opening.

DOSAGE & ADMINISTRATION SECTION

for topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72945-0002-22023-01-30C16284748780-1f386c649-e22b-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72945-0002-1CURITHYS5 mg in 1 PATCHPATCH54
72945-0002-2CURITHYS6 in 1 POUCHPATCH64

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72945-0002CURITHYS (SODIUM HYALURONATE) PATCH [J WORLD]4Legacy NDC, 2 package rows20211202_8e2aae94-010f-6e6e-e053-2a95a90a2859.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72945-000272945-0002-1, 72945-0002-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4IACT
HYALURONATE SODIUMYSE9PPT4THACTIB

Source Document#

Source XML · Source PDF

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
d20fa805-ab77-8d84-e053-2a95a90a3c178e2aae94-010f-6e6e-e053-2a95a90a28592021-12-01WarningsExact identifier
spl id: d20fa805-ab77-8d84-e053-2a95a90a3c17
spl set id: 8e2aae94-010f-6e6e-e053-2a95a90a2859

Reported adverse events (FAERS/openFDA)#

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