Label: NATURALTH GOAT MILK MOISTURE ESSENCE- dimethicone cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 59078-290-01, 59078-290-02 - Packager: TONYMOLY 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 May 27, 2016
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive Ingredient: Water, Goat Milk Extract, Hydrogenated Polydecene, Butylene Glycol, Cetyl Ethylhexanoate, 1,2-Hexanediol, Polysorbate 60, Butyrospermum Parkii (Shea) Butter, Glyceryl Stearate, Panthenol, Cetearyl Alcohol, Polyglyceryl-3 Methylglucose Distearate, Biosaccharide Gum-1, Phenoxyethanol, Sorbitan Stearate, Dimethicone, Palmitic Acid, Carbomer, PEG-100 Stearate, Stearic Acid, Tromethamine, Polyacrylate-13, Polyisobutene, Ethylhexylglycerin, Xanthan Gum, Fragrance, Disodium EDTA, Polysorbate 20, Pantolactone, Sorbitan Isostearate, Lecithin, Alcohol, Polysorbate 80, Sodium Ascorbyl Phosphate, Ceramide 3, Anthocyanins, Citric Acid, Hydrolyzed Hyaluronic Acid
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Use
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NATURALTH GOAT MILK MOISTURE ESSENCE
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59078-290 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone 0.8 g in 50 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:59078-290-02 1 in 1 CARTON 05/01/2016 1 NDC:59078-290-01 50 mL in 1 BOTTLE, PUMP; 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 05/01/2016 Labeler - TONYMOLY CO.,LTD (688216798) Registrant - TONYMOLY CO.,LTD (688216798) Establishment Name Address ID/FEI Business Operations TONYMOLY CO.,LTD 688216798 manufacture(59078-290)