FDA.reportPublic FDA data

KAEWOON FOR MEN

Manufacturer
RNCARE
Effective date
2021-10-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:42:37

Label at a glance#

ProductKAEWOON FOR MEN
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, Polyquaternium-10 , Hydroxyethylcellulose , Black Strap Powder , Oleic Acid , Menthol , Lauryl Glucoside , Polysorbate 85 , 1,2-Hexanediol , Caprylic/Capric Triglyceride , Oryza Sativa (Rice) Bran Extract , Curcuma Longa (Turmeric Root) Extract, Vigna Radiata Seed Extract , Artemisia Princeps Extract , Arctium Lappa Root Extract , Hippophae Rhamnoides Extract , Hawthorn Crataegus Cuneata Extract Rheum Palmatum Root Extract , Bambusa Vulgaris Extract, Hamamelis Virginiana (Witch Hazel) Extract , Chamomilla Recutita (Matricaria) Extract , Panax Ginseng Root Extract , Propolis Extract , Sapindus Mukurossi Fruit Extract , Disodium EDTA , Diglycerin , Hydrolyzed Collagen , Butylene Glycol , Lauramidopropyl Betaine , Shea Butteramidopropyl Betaine , Capryl/Capramidopropyl Betaine , Sodium Cocoamphoacetate , 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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71237-003-022023-01-30C16284748780-1ba0f9c33-3603-a910-e053-dadaa90a0b8571237-003_V2
71237-003-022021-10-04C16284748780-1ba0f9c33-3603-a910-e053-dadaa90a0b8571237-003_V2
71237-003-022021-01-29C16284748780-1ba0f9c33-3603-a910-e053-dadaa90a0b8571237-003_V2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71237-003-01KAEWOON FOR MEN320 mL in 1 BOTTLEGEL3203
71237-003-02KAEWOON FOR MEN1 in 1 CARTONGEL13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71237-003KAEWOON FOR MEN (HYALURONIC ACID, ALLANTOIN) GEL [RNCARE]3Legacy NDC, 2 package rows20211005_9849acaf-8045-411d-9ca1-797ca41ef4e5.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71237-00371237-003-01, 71237-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYALURONIC ACIDS270N0TRQYACTIB
ALLANTOIN344S277G0ZACTIB
WATER059QF0KO0RIACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)GMR4PEN8PKIACT
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)R33S7TK2EPIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
POLYSORBATE 85A7F3N56197IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
RICE BRANR60QEP13ICIACT
TURMERIC856YO1Z64FIACT
MUNG BEAN1LIB31N73GIACT
ARCTIUM LAPPA ROOT597E9BI3Z3IACT
HIPPOPHAE RHAMNOIDES SEEDZD5PJT4UZFIACT
RHEUM PALMATUM ROOTG025DAL7CEIACT
BAMBUSA VULGARIS WHOLEWCD45M1BSKIACT
HAMAMELIS VIRGINIANA LEAF WATER8FP93ED6H2IACT
MATRICARIA CHAMOMILLA ROOTBTG5H50X7FIACT
SAPINDUS MUKOROSSI FRUIT66H9NW427YIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
LAURAMIDOPROPYL BETAINE23D6XVI233IACT
SODIUM COCOAMPHOACETATEW7Q5E87674IACT

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
cd8b0563-db24-db8c-e053-2995a90a88169849acaf-8045-411d-9ca1-797ca41ef4e52021-10-04WarningsExact identifier
spl id: cd8b0563-db24-db8c-e053-2995a90a8816
spl set id: 9849acaf-8045-411d-9ca1-797ca41ef4e5

Reported adverse events (FAERS/openFDA)#

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