OTC Medication Information: KAEWOON FOR WOMEN

KAEWOON FOR WOMEN- hyaluronic acid and 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.

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 Type HUMAN OTC DRUG Item Code (Source) NDC:71237-004
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYALURONIC ACID (HYALURONIC ACID) HYALURONIC ACID 20 mg in 1 mL
ALLANTOIN (ALLANTOIN) ALLANTOIN 2 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
SODIUM COCOATE
OLEIC ACID
COCO MONOISOPROPANOLAMIDE
DIGLYCERIN
BUTYLENE GLYCOL
POLYSORBATE 85
1,2-HEXANEDIOL
SODIUM COCOAMPHOACETATE
RICE BRAN
GREEN TEA LEAF
TURMERIC
ARCTIUM LAPPA ROOT
HIPPOPHAE RHAMNOIDES SEED
RHEUM PALMATUM ROOT
BAMBUSA VULGARIS WHOLE
HAMAMELIS VIRGINIANA LEAF WATER
MATRICARIA CHAMOMILLA ROOT
SAPINDUS MUKOROSSI FRUIT
EDETATE DISODIUM ANHYDROUS
MENTHOL, UNSPECIFIED FORM
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71237-004-02 1 BOTTLE in 1 CARTON contains a BOTTLE (71237-004-01)
1 NDC:71237-004-01 320 mL in 1 BOTTLE This package is contained within the CARTON (71237-004-02)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 11/21/2018
Labeler — RNCARE (694893883)
Registrant — RNCARE (694893883)
Establishment
Name Address ID/FEI Operations
RNCARE 694893883 manufacture (71237-004)

Revised: 12/2019 RNCARE

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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