- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INACTIVE INGREDIENT
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
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
KAEWOON FOR MEN
hyaluronic acid, allantoin gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71237-003 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) POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK) HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) POLYSORBATE 85 (UNII: A7F3N56197) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) RICE BRAN (UNII: R60QEP13IC) TURMERIC (UNII: 856YO1Z64F) MUNG BEAN (UNII: 1LIB31N73G) 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) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233) SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71237-003-02 1 in 1 CARTON 11/21/2018 1 NDC:71237-003-01 320 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(71237-003)