- ACTIVE INGREDIENT
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INACTIVE INGREDIENT
Inactive ingredient : WATER, GLYCERIN, HYDROGENATED POLYDECENE, HUMAN BONE MARROW STEM CELL CONDITIONED MEDIA, DIPROPYLENE GLYCOL, CETEARYL ALCOHOL, POLYGLYCERYL-3 METHYLGLUCOSE DISTEARATE, BUTYROSPERMUM PARKII(SHEA BUTTER), DIPENTAERYTHRITYL HEXA C5-9 ACID ESTERS, BETAINE, GLYCERYL STEARATE SE, CITRUS PARADISI (GRAPEFRUIT) FRUIT EXTRACT, STEARIC ACID, POLYGONUM MULTIFLORUM ROOT EXTRACT, ACANTHOPANAX SENTICOSUS (ELEUTHERO) ROOT EXTRACT, PORTULACA OLERACEA EXTRACT, PANAX GINSENG ROOT EXTRACT, ASPARAGUS COCHINCHINENSIS ROOT EXTRACT, TOCOPHERYL ACETATE, PHENOXYETHANOL, CARBOMER, 1,2-HEXANEDIOL, BEESWAX, XANTHAN GUM, GLYCERYL STEARATE, PEG-100 STEARATE, HYDROGENATED LECITHIN, ALTHAEA ROSEA ROOT EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, GANODERMA LUCIDUM (MUSHROOM) EXTRACT, GRIFOLA FRONDOSA EXTRACT, INONOTUS OBLIQUUS (MUSHROOM) EXTRACT, SPARASSIS CRISPA EXTRACT, PHELLINUS LINTEUS EXTRACT, POTASSIUM HYDROXIDE, CERAMIDE 3, ADENOSINE, SODIUM HYALURONATE, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL, EUCALYPTUS GLOBULUS LEAF OIL, GERANIUM MACULATUM OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL, MENTHA PIPERITA (PEPPERMINT) OIL
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS AND USAGE
- DOSAGE AND ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
BY PHARMICELL LAB LUXURY CELL PERFORMANCE EYE
dimethicone creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:60949-070 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 20 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:60949-070-01 20 g in 1 CARTON Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/01/2013 Labeler - Pharmicell Co., Ltd. (687744110) Registrant - Pharmicell Co., Ltd. (687744110) Establishment Name Address ID/FEI Business Operations Pharmicell Co., Ltd. 687744110 manufacture(60949-070)