KAEWOON FOR WOMEN

Manufacturer
RNCARE
Effective date
2021-10-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:42:36

Label at a glance#

ProductKAEWOON FOR WOMEN
Active ingredientHYALURONIC ACID, ALLANTOIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

HYALURONIC ACID 2%

Allantoin 0.2%

OTC - PURPOSE SECTION

Skin Protectant

INDICATIONS & USAGE SECTION

Body Cleansing

DOSAGE & ADMINISTRATION SECTION

Take an appropriate amount and massage onto body for about 60 seconds and rinse with water

WARNINGS SECTION

In case of eye contact, immediately rinse with water

Stop use if unusual redness, swelling, soreness or irritation occur

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INACTIVE INGREDIENT SECTION

Water, Sodium Cocoate, Oleic Acid, Cocamide MIPA, DiGlycerin, Butylene Glycol, Shea Butteramidopropyl Betaine, Hydrolyzed Collagen, Polysorbate85, 1,2-Hexanediol, Sodium Cocoamphoacetate, Oryza Sativa (Rice) Bran Extract, Camellia Sinensis Leaf Extract, Black Strap Powder, Curcuma Longa (Turmeric) Root Extract, Phaseolus Radiatus Seed Extract, Artemisia Vulgaris Extract, Arctium Lappa Root Extract, Hippophae Rhamnoides Extract, Crataegus Oxyacantha Extract, Rheum Palmatum Root Extract, Bambusa Vulgaris Extract, Eucalyptus Globulus Leaf Extract, Hamamelis Virginiana (Witch Hazel) Extract, Chamomilla Recutita (Matricaria) Flower/Leaf Extract, Sapindus Mukorossi Fruit Extract, Capryl/Capramidopropyl Betaine, Caprylic/Capric Triglycerid, Polyquaternium-10, Panax Ginseng Root Extract, Hydroxyethylcellulose, Disodium EDTA, Menthol, Mandelic Acid, Propolis Extract, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2104187allantoin 0.2 % / hyaluronic acid 2 % Medicated Liquid SoapPSN3
2104187allantoin 2 MG/ML / hyaluronic acid 20 MG/ML Medicated Liquid SoapSCD3
2104187allantoin 0.2 % / hyaluronic acid 2 % Medicated Liquid SoapSY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71237-004-022023-01-30C16284748780-1ba0f9c33-3600-a910-e053-dadaa90a0b8571237-004_V2
71237-004-022021-10-04C16284748780-1ba0f9c33-3600-a910-e053-dadaa90a0b8571237-004_V2
71237-004-022021-01-29C16284748780-1ba0f9c33-3600-a910-e053-dadaa90a0b8571237-004_V2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71237-004-01KAEWOON FOR WOMEN320 mL in 1 BOTTLEGEL3203
71237-004-02KAEWOON FOR WOMEN1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71237-004KAEWOON FOR WOMEN (HYALURONIC ACID, ALLANTOIN) GEL [RNCARE]3Legacy NDC, 2 package rows20211005_05fc4bf9-49fc-4844-887d-3fcb624f9c37.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71237-00471237-004-01, 71237-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 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
cd8af91d-0b47-b3e5-e053-2995a90a638e05fc4bf9-49fc-4844-887d-3fcb624f9c372021-10-04WarningsExact identifier
spl id: cd8af91d-0b47-b3e5-e053-2995a90a638e
spl set id: 05fc4bf9-49fc-4844-887d-3fcb624f9c37

Reported adverse events (FAERS/openFDA)#

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