Label: GINSENG WHITENING- niacinamide cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70969-101-01, 70969-101-02 - Packager: Synbio 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 September 19, 2016
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Keep out of reach of children
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Warnings
For external use only
Do not use when Your skin is red, inflamed, irritated or painful
When using this product
- Do not apply on other parts of the body
- Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
- Do not apply directly to wound or open cut.
Stop use and ask doctor if rash or irritation on skin develops and lasts.
Store at room temperature - Directions
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Inactive Ingredients
D.I. Water, 1,3 Butylene Glycol, Cethylethyl Hexanoate, Glycerin, Caprylic/Capric Triglyceride, Glyceryl Oleate, Cetearyl Alcohol, Lecithin, Glyceryl Stearate, Tranexamic Acid, 1,2 Hexandiol, Ginsenoside, Glycerylstearate, PEG-100 Stearate, Polyglyceryl -3, Methylglucos Distearate, Citrus Paradisi (Grapefruit) Fruit Extract, Sodium Hyaluronate, Dimethicone, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Arnica Montana Flower Extract, Portulaca Oleracea Extract, Camellia Sinensis Leaf Extract, Poloxamer 407, Polysorbate 80, Isohexadecane, Phenoxyethanol, Citric Acid, Perfume
- Ginseng Whitening Cream
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INGREDIENTS AND APPEARANCE
GINSENG WHITENING
niacinamide creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70969-101 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Niacinamide (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) Niacinamide 2 g in 50 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CETYL ETHYLHEXANOATE (UNII: 134647WMX4) Glycerin (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) Glyceryl Oleate (UNII: 4PC054V79P) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) TRANEXAMIC ACID (UNII: 6T84R30KC1) 1,2-HEXANEDIOL (UNII: TR046Y3K1G) GINSENOSIDES (UNII: 3K198YD54P) PEG-100 STEARATE (UNII: YD01N1999R) POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6) GRAPEFRUIT (UNII: O82C39RR8C) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Dimethicone (UNII: 92RU3N3Y1O) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) PURSLANE (UNII: M6S840WXG5) GREEN TEA LEAF (UNII: W2ZU1RY8B0) POLOXAMER 407 (UNII: TUF2IVW3M2) POLYSORBATE 80 (UNII: 6OZP39ZG8H) ISOHEXADECANE (UNII: 918X1OUF1E) PHENOXYETHANOL (UNII: HIE492ZZ3T) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70969-101-02 1 in 1 PACKAGE 09/19/2016 1 NDC:70969-101-01 50 g in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/19/2016 Labeler - Synbio Co., Ltd. (557821393) Registrant - Synbio Co., Ltd. (557821393) Establishment Name Address ID/FEI Business Operations Synbio Co., Ltd. 557821393 manufacture(70969-101)