CURESTIN

Manufacturer: J World | DS TECH CO., LTD
Effective date: 2019-07-31
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:59:58

Label at a glance#

ProductCURESTIN

Active ingredientHYALURONATE SODIUM

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium hyaluronate

INACTIVE INGREDIENT SECTION

Acetyl Hexapeptide-8

OTC - PURPOSE SECTION

Premium skin care products that work on tired skin and give shine and vitality

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

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72945-0001-1	2023-01-30	C162847	48780-1	f386c649-c02c-0266-e053-dadaa90a7c1a	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72945-0001-1	CURESTIN	10 mg in 1 POUCH	PATCH	10		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72945-0001	CURESTIN (ZINC PYRITHIONE, SALICYLIC ACID) PATCH [J WORLD]	3	Legacy NDC, 1 package rows	20190731_8e254574-dd4c-3fe4-e053-2a95a90a27c7.zip

Products#

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

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

CURESTIN
Zinc Pyrithione, salicylic acid
HYALURONATE SODIUM
HYALURONIC ACID
ACETYL HEXAPEPTIDE-8

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72945-0001	72945-0001-1

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
Name	UNII	Kind
HYALURONATE SODIUM	YSE9PPT4TH	ACTIB
ACETYL HEXAPEPTIDE-8	L4EL31FWIL	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d20fa805-ab6d-8d84-e053-2a95a90a3c17			8e254574-dd4c-3fe4-e053-2a95a90a27c7	2021-12-01	Warnings	Exact identifier spl set id: 8e254574-dd4c-3fe4-e053-2a95a90a27c7

Reported adverse events (FAERS/openFDA)#

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