KAEWOON FOR WOMEN- hyaluronic acid, allantoin gel 
RNCARE

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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71237-004_V2

HYALURONIC ACID 2%

Allantoin 0.2%

Skin Protectant

Body Cleansing

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

In case of eye contact, immediately rinse with water

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

Keep out of reach of children

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

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KAEWOON FOR WOMEN 
hyaluronic acid, allantoin gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71237-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID20 mg  in 1 mL
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN2 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM COCOATE (UNII: R1TQH25F4I)  
OLEIC ACID (UNII: 2UMI9U37CP)  
COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
DIGLYCERIN (UNII: 3YC120743U)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
POLYSORBATE 85 (UNII: A7F3N56197)  
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)  
RICE BRAN (UNII: R60QEP13IC)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
TURMERIC (UNII: 856YO1Z64F)  
ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
HIPPOPHAE RHAMNOIDES SEED (UNII: ZD5PJT4UZF)  
RHEUM PALMATUM ROOT (UNII: G025DAL7CE)  
BAMBUSA VULGARIS WHOLE (UNII: WCD45M1BSK)  
HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)  
MATRICARIA CHAMOMILLA ROOT (UNII: BTG5H50X7F)  
SAPINDUS MUKOROSSI FRUIT (UNII: 66H9NW427Y)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71237-004-021 in 1 CARTON11/21/2018
1NDC:71237-004-01320 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other11/21/2018
Labeler - RNCARE (694893883)
Registrant - RNCARE (694893883)
Establishment
NameAddressID/FEIBusiness Operations
RNCARE694893883manufacture(71237-004)

Revised: 10/2021
Document Id: cd8af91d-0b47-b3e5-e053-2995a90a638e
Set id: 05fc4bf9-49fc-4844-887d-3fcb624f9c37
Version: 3
Effective Time: 20211004
 
RNCARE