Label: TONYMOLY NATURALTH GOAT MILK PREMIUM- dimethicone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 59078-250-01 - Packager: TONYMOLY CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 January 20, 2016
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- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredients: goat milk extract, glycerin, cyclopentasiloxane, propanediol, niacinamide, dimethicone/peg-10/15 crosspolymer, sodium chloride, piper methysticum leaf/root/stem extract, peg-10 dimethicone, peg-9 polydimethylsiloxyethyl dimethicone, aloe barbadensis leaf juice, titanium dioxide, arctium lappa root extract, phellinus linteus extract, xanthan gum, phenoxyethanol, soluble collagen, hydrogenated lecithin, sodium hyaluronate, sodium citrate, portulaca oleracea extract, pueraria thunbergiana root, cnidium officinale root, glycyrrhiza glabra (licorice), paeonia lactiflora root, mannitol, ethylhexylglycerin, mica, water, fragrance, adenosine, butylene glycol, peg-12, ethylcellulose, hydroxypropyl methylcellulose, hydrolyzed hyaluronic acid, folic acid, ceramide 3, cholesterol, raffinose, tromethamine, iron oxides(ci77491), iron oxides(ci77492), panthenol, palmitoyl pentapeptide-4
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- Use
- Directions
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
TONYMOLY NATURALTH GOAT MILK PREMIUM
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59078-250 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Dimethicone (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) Dimethicone 0.6 g in 60 mL Inactive Ingredients Ingredient Name Strength goat milk (UNII: XE5K5I4RP7) glycerin (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59078-250-01 60 mL in 1 CARTON; 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 12/01/2015 Labeler - TONYMOLY CO.,LTD (688216798) Registrant - TONYMOLY CO.,LTD (688216798) Establishment Name Address ID/FEI Business Operations TONYMOLY CO.,LTD 688216798 manufacture(59078-250)