Label: NATURALTH GOAT MILK PREMIUM TONE UP- glycerin, niacinamide cream
-
Contains inactivated NDC Code(s)
NDC Code(s): 59078-301-01, 59078-301-02 - Packager: TONYMOLY CO.,LTD
- 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 May 27, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
Inactive Ingredient: Goat Milk Extract, Dipropylene Glycol, Water, Cyclopentasiloxane, PEG/PPG-17/6 Copolymer, Butylene Glycol, Titanium Dioxide (CI 77891), Bis-PEG-18 Methyl Ether Dimethyl Silane, Cyclohexasiloxane, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Isohexadecane, Phenoxyethanol, Sodium Polyacrylate, Polysorbate 80, Dimethiconol, Chlorphenesin, Ethylhexylglycerin, Caprylyl Glycol, Triethoxycaprylylsilane, Fragrance, Disodium EDTA, Bifida Ferment Lysate, 1,2-Hexanediol, Lecithin, Alcohol, Hydrolyzed Collagen, Nelumbo Nucifera Flower Extract, Hydrolyzed Hyaluronic Acid, Lactobacillus Ferment, Sodium Ascorbyl Phosphate, Anthocyanins
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Use
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
NATURALTH GOAT MILK PREMIUM TONE UP
glycerin, niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59078-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) Glycerin 9.3 g in 60 mL Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 1.2 g in 60 mL Inactive Ingredients Ingredient Name Strength Dipropylene Glycol (UNII: E107L85C40) Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59078-301-02 1 in 1 CARTON 05/01/2016 1 NDC:59078-301-01 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 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(59078-301)