LIGHTENING DAY CREAM- dicaprylyl carbonate cream
LANGE SAS

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.

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KEY ACTIVE INGREDIENTS
Seaweed, Licorice Root and White Tea Extract

This Whitening Seaweed inhibits melanin synthesis and reduces pigmentation of synthesized melanins with elimination of pigmented scales.

Keep out of reach of children.

LIGHTENING DAY CREAM LANGE
A light and moisturizing cream, to help:
Inhibit skin pigmentation,
Nourish and moisturize the skin.

WARNING!
Avoid contact with the eyes;
Avoid or afford protecting from UV
whilst using products containing AHA
because of the suggestion of susceptibility to
increased damage from UV.

50 mL
1.7 FL. OZ

WATER (AQUA)
GLYCERIN
PEG-8
DICAPRYLYL CARBONATE
GLYCERYL STEARATE SE
ISONONYL ISONONANOATE
CAMELLIA KISSI SEED OIL
DIMETHICONE
POLYACRYLAMIDE
PHENOXYETHANOL
PROPYLENE GLYCOL
CETYL ALCOHOL
STEARIC ACID
XANTHAN GUM
C13-14 ISOPARAFFIN
SODIUM PCA
DISODIUM EDTA
PROPYLPARABEN
METHYLPARABEN
LAURETH-7
MAGNESIUM ASCORBYL PHOSPHATE
MENTHOXYPROPANEDIOL
o-CYMEN-5-OL
GLYCERYL POLYACRYLATE
GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER
ETHYLPARABEN
GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT
BUTYLENE GLYCOL

LANGE
PARIS
LIGHTENING DAY CREAM
Morning radiance with Seaweed extracts
50 ml
1.7 FL. OZ

LIGHTENING DAY CREAM
dicaprylyl carbonate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:51830-019
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) (POLYETHYLENE GLYCOL 400 - UNII:B697894SGQ)	POLYETHYLENE GLYCOL 400	2.5 mg in 50 mg

Ingredient Name	Strength
Inactive Ingredients
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
CAMELLIA KISSII SEED OIL (UNII: 96HGN0T99A)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
CETYL ALCOHOL (UNII: 936JST6JCN)
STEARIC ACID (UNII: 4ELV7Z65AP)
XANTHAN GUM (UNII: TTV12P4NEE)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
METHYLPARABEN (UNII: A2I8C7HI9T)
LAURETH-7 (UNII: Z95S6G8201)
3-((L-MENTHYL)OXY)PROPANE-1,2-DIOL (UNII: KD6TZ2QICH)
O-CYMEN-5-OL (UNII: H41B6Q1I9L)
ETHYLPARABEN (UNII: 14255EXE39)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
GLYCERIN (UNII: PDC6A3C0OX)
ACRYLIC ACID (UNII: J94PBK7X8S)
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:51830-019-04	50 mg in 1 CONTAINER

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		07/18/2012

Labeler - LANGE SAS (275956105)

Registrant - LANGE SAS (275956105)

Name	Address	ID/FEI	Business Operations
Establishment
LANGE SAS		275956105	manufacture(51830-019)