Label: KAEWOON FOR MEN- hyaluronic acid, allantoin gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71237-003-01, 71237-003-02 - Packager: RNCARE
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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.
Drug Label Information
Updated October 4, 2021
If you are a consumer or patient please visit this version.
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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, 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)
