Label: DOCTORCOS SNOW WHITE WATER GLOW MASK- dimethicone cream
- NDC Code(s): 71121-010-01, 71121-010-02
- Packager: DOCTORCOS CO., LTD
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated August 11, 2017
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive Ingredients: Water, Cyclopentasiloxane, Butylene Glycol, PEG-32, Sodium Hyaluronate, Cyclomethicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Niacinamide, Sodium Chloride, 1,2-hexandiol, Cetyl PEG/PPG-10/1 Dimethicone, Portulaca Oleracea Extract, Betaine, Tocopheryl Acetate, Ethylhexylglycerin, Centella Asiatica Extract, Adenosine, Disodium EDTA, Dipotassium Glycyrrhizate, Fragrance, Hyaluronic Acid, Allantoin, Aloe Barbadensis Leaf Extract, Calcium Pantothenate, Sodium Ascorbyl Phosphate, Tocopheryl Acetate, Pyridoxine HCl, Maltodextrin, Sodium Starch Octenylsuccinate, Silica, Camellia Japonica Seed Oil, Camellia Sinensis Leaf Extract, Royal Jelly Extract, Propolis Extract, Hydrolyzed Royal Jelly Protein, Acacia Concinna Fruit Extract, Hydrolyzed Collagen, Hydrolyzed Elastin, Ceramide NP, Morus Alba Bark Extract, Galactomyces Ferment Filtrate, Malpighia Emarginata (Acerola) Fruit Extract, Litchi Chinensis Fruit Extract, Glycerin, Glycereth-26, Copper Tripeptide-1, rh-Oligopeptide-1, Acetyl Hexapeptide-8
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
Indications & usage: After washing your face, apply suitable amount of the product to your face. About 15 to 20 minutes later, do not scrub but let it absorbed as it is.(In case of using the product at nighttime before you sleep, massage gently or tap your fingers on the face to help it absorbed deeply.).
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
DOCTORCOS SNOW WHITE WATER GLOW MASK
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71121-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone 5.5 g in 110 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Butylene Glycol (UNII: 3XUS85K0RA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71121-010-02 1 in 1 CARTON 11/01/2016 1 NDC:71121-010-01 110 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 OTC monograph final part347 11/01/2016 Labeler - DOCTORCOS CO., LTD (689060756) Registrant - DOCTORCOS CO., LTD (689060756) Establishment Name Address ID/FEI Business Operations Miz Herb 688216078 manufacture(71121-010)
