TOMATO WHITENING SERUM- dimethicone cream

TOMATO WHITENING SERUM by

Drug Labeling and Warnings

TOMATO WHITENING SERUM by is a Otc medication manufactured, distributed, or labeled by SKINFOOD CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient: DIMETHICONE

INACTIVE INGREDIENT

Inactive ingredients:

WATER, GLYCERETH-26, ISOHEXADECANE, ARBUTIN, SOLANUM LYCOPERSICUM (TOMATO) FRUIT/LEAF/STEM EXTRACT, ISOSTEARYL NEOPENTANOATE, DIETHOXYETHYL SUCCINATE, BIS-PEG-18 METHYL ETHER DIMETHYL SILANE, SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, POLYSORBATE 80, C14-22 ALCOHOLS, C12-20 ALKYL GLUCOSIDE, STEARIC ACID, HYDROGENATED LECITHIN, GLYCERYL STEARATE SE, CETEARYL ALCOHOL, PUNICA GRANATUM EXTRACT, HONEY EXTRACT, HYDROXYETHYL UREA, CHAENOMELES SINENSIS FRUIT EXTRACT, BUTYLENE GLYCOL, ALCOHOL DENAT., DIACETYL BOLDINE, ARGININE, CARBOMER, CAPRYLIC/CAPRIC TRIGLYCERIDE, DISODIUM EDTA, TOCOPHERYL ACETATE, METHYLPARABEN, PROPYLPARABEN, PHENOXYETHANOL, FRAGRANCE

PURPOSE

Purpose:

This combination of cosmetics is used for your basic skin care and gives a benefit for skin Brightening care.

WARNINGS

Warnings:

For external use only. Avoid contact with eyes. Discontinue use if signs of irritation appear.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children:

Keep out of reach of children

INDICATIONS & USAGE

Indication and usage:

Following toner, pour some on the palm of your hand and apply to skin gently. Press down lightly until absorbed.

DOSAGE & ADMINISTRATION

Dosage and administration:

Take appropriate amount according to your skin condition and apply every morning and night.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TOMATO WHITENING SERUM 
dimethicone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76214-005
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	0.35 mL  in 35 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERETH-26 (UNII: NNE56F2N14)
ISOHEXADECANE (UNII: 918X1OUF1E)
ARBUTIN (UNII: C5INA23HXF)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
C14-22 ALCOHOLS (UNII: B1K89384RJ)
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
STEARIC ACID (UNII: 4ELV7Z65AP)
METHYLPARABEN (UNII: A2I8C7HI9T)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
POMEGRANATE (UNII: 56687D1Z4D)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HONEY (UNII: Y9H1V576FH)
HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
CHAENOMELES SPECIOSA FRUIT (UNII: 6S5Q1Q537Z)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ARGININE (UNII: 94ZLA3W45F)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76214-005-01	35 mL in 1 CARTON

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	03/01/2011

Labeler - SKINFOOD CO., LTD. (690324173)

Registrant - SKINFOOD CO., LTD. (690324173)

Establishment
Name	Address	ID/FEI	Business Operations
SKINFOOD CO., LTD.		690324173	manufacture