Label: KAEWOON FOR WOMEN- hyaluronic acid, allantoin gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71237-004-01, 71237-004-02 - Packager: RNCARE
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated October 4, 2021
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KAEWOON FOR WOMEN
hyaluronic acid, allantoin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71237-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONIC ACID 20 mg in 1 mL ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) ALLANTOIN 2 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:71237-004-02 1 in 1 CARTON 11/21/2018 1 NDC:71237-004-01 320 mL in 1 BOTTLE; Type 0: Not a Combination Product 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 Business Operations RNCARE 694893883 manufacture(71237-004)
