Label: WRINKLESS PLUS CT-1 LIFTING UP ESSENCE- dimethicone cream
Contains inactivated NDC Code(s)
NDC Code(s): 44781-120-01
- Packager: ZION SYNTHETIC FIBER 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 August 29, 2011
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
Water, Caprilic Capric Triglyceride, Glycerin, Butylene Glycol, Propylene Glycol Dicaprylate Dicaprate, Cetearyl Olivate, Sorbitan Olivate, Butylene Glycol Dicaprylate/Dicaprate, Glycine Soja (Soybean) Oil, Cetearyl Alcohol, Saccharide Isomerate, Bees Wax, Hydrogenated Lecithin, Limnanthes Alba (Meadowfoam) Seed Oil, Portulaca Oleracea Extract, Solanum Lycopersicum (Tomato)Fruit Extract, Vitis Vinifera(Grape) Seed Extract, Glyceryl Stearate, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Amethyst Powder, Topaz, Aluminum Silicate, Zeolite, Hematite Extract, Palmitoyl Pentapeptide-4, Ubiquinone, Carbomer, Isononyl Isononanoate, Triethanolamine, Tocopheryl Acetate, Allantoin, Betula Alba Juice, Panax Ginseng Root Extract, Calendula Officinalis Flower Extract, Angelica Keiskei Leaf/Stem Extract, Punica Granatum Fruit Extract, Pinus Sylvestris Bud Extract, Polygonum Multiflorum Root Extract, Solanum Tuberosum (Potato) Pulp Extract, Artemisia Vulgaris Extract,
Ginkgo Biloba Leaf Extract, Vigna Radiata Seed Extract, Propolis Extract, Disodium EDTA, Adenosine, Xanthan Gum, Polysorbate 20, Sodium Hyaluronate, Sodium Polyacrylate, Methyl Paraben, Butyl Paraben, Flavor
In case of having following symptoms after using this, you're advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist.
- In case of having problems such as red rash, swollenness, itching, stimulation during usage.
- In case of having the same symptoms above on the part you put this product on by direct sunlight.
You are banned to use it on the part where you have a scar, eczema, or dermatitis.
In case of getting it into your eyes, you have to wash it immediately.
- KEEP OUT OF REACH OF CHILDREN
INDICATIONS & USAGE
Indications and Usage:
Tighten the lid after using it.
Don't keep it in the place where the temperature is extremely hot or low and exposed the direct sunlight.
Please apply it an adequate quantity evenly on face, throat, arms and legs at the last stage of basic makeup.
Please apply it once again on your skin at the time when you're going out, sports activity, and any activities of outside.
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
WRINKLESS PLUS CT-1 LIFTING UP ESSENCE
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44781-120 Route of Administration CUTANEOUS Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 0.45 mL in 45 mL Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Glycerin (UNII: PDC6A3C0OX) Butylene Glycol (UNII: 3XUS85K0RA) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SOYBEAN OIL (UNII: 241ATL177A) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y) TOMATO (UNII: Z4KHF2C175) WINE GRAPE (UNII: 3GOV20705G) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) ALUMINUM SILICATE (UNII: T1FAD4SS2M) UBIDECARENONE (UNII: EJ27X76M46) CARBOMER 934 (UNII: Z135WT9208) TROLAMINE (UNII: 9O3K93S3TK) ALLANTOIN (UNII: 344S277G0Z) CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) POTATO (UNII: CFE1S8DYWD) ARTEMISIA VULGARIS POLLEN (UNII: ANT994T71D) POLYSORBATE 20 (UNII: 7T1F30V5YH) HYALURONATE SODIUM (UNII: YSE9PPT4TH) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYLPARABEN (UNII: 3QPI1U3FV8) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:44781-120-01 45 mL in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 04/01/2010 Labeler - ZION SYNTHETIC FIBER CO., LTD. (688011147) Registrant - ZION SYNTHETIC FIBER CO., LTD. (688011147) Establishment Name Address ID/FEI Business Operations ZION SYNTHETIC FIBER CO., LTD. 688011147 manufacture