Label: LIGHTENING NIGHT CREAM- ethyl macadamiate cream
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Contains inactivated NDC Code(s)
NDC Code(s): 51830-020-05 - Packager: LANGE SAS
- Category: HUMAN OTC DRUG LABEL
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 July 18, 2012
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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INACTIVE INGREDIENT
WATER
PEG-8
GLYCERIN
CAPRYLIC/CAPRIC TRIGLYCERIDE
ARACHIDYL ALCOHOL
METHYL GLUCETH-20
ETHYL MACADAMIATE
BEHENYL ALCOHOL
CAMELLIA KISSI SEED OIL
HEXYLDECANOL
HEXYLDECYL LAURATE
SODIUM POLYACRYLATE
PROPYLENE GLYCOL
CYCLOPENTASILOXANE
ARACHIDYL GLUCOSIDE
PHENOXYETHANOL
HYDROGENATED COCONUT OIL
SODIUM PCA
DISODIUM EDTA
PROPYLPARABEN
DIMETHICONOL
METHYLPARABEN
MAGNESIUM ASCORBYL PHOSPHATE
o-CYMEN-5-OL
TROMETHAMINE
ETHYLPARABEN
GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT
CITRUS NOBILIS (MANDARIN ORANGE) FRUIT EXTRACT
GLYCERYL ACRYLATE/ACRYLIC ACID COPOLYMER
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL
BUTYLENE GLYCOL
TOCOPHEROL
GLYCERYL POLYACRYLATE
BAMBUSA VULGARIS EXTRACT
PANAX GINSENG ROOT EXTRACT
GARDENIA TAHITENSIS FLOWER
IRIS FLORENTINA ROOT EXTRACT
ASCOPHYLLUM NODOSUM EXTRACT - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LIGHTENING NIGHT CREAM
ethyl macadamiate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51830-020 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ETHYL MACADAMIATE (UNII: ANA2NCS6V1) (ETHYL MACADAMIATE - UNII:ANA2NCS6V1) ETHYL MACADAMIATE 1 mg in 50 mg Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) GLYCERIN (UNII: PDC6A3C0OX) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) METHYL GLUCETH-20 (UNII: J3QD0LD11P) DOCOSANOL (UNII: 9G1OE216XY) CAMELLIA KISSII SEED OIL (UNII: 96HGN0T99A) HEXYLDECANOL (UNII: 151Z7P1317) HEXYLDECYL LAURATE (UNII: 0V595C1P6M) SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) PHENOXYETHANOL (UNII: HIE492ZZ3T) HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM) SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2) EDETATE DISODIUM (UNII: 7FLD91C86K) PROPYLPARABEN (UNII: Z8IX2SC1OH) DIMETHICONOL (100000 CST) (UNII: OSA9UP217S) METHYLPARABEN (UNII: A2I8C7HI9T) MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5) O-CYMEN-5-OL (UNII: H41B6Q1I9L) TROMETHAMINE (UNII: 023C2WHX2V) ETHYLPARABEN (UNII: 14255EXE39) GLYCYRRHIZA GLABRA (UNII: 2788Z9758H) TANGERINE (UNII: KH3E3096OO) ACRYLIC ACID (UNII: J94PBK7X8S) SUNFLOWER OIL (UNII: 3W1JG795YI) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TOCOPHEROL (UNII: R0ZB2556P8) BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V) ASIAN GINSENG (UNII: CUQ3A77YXI) GARDENIA TAITENSIS FLOWER (UNII: T0OCU8201Y) IRIS GERMANICA VAR. FLORENTINA ROOT (UNII: M30XO5X4XD) ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51830-020-05 50 mg in 1 BOX Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/18/2012 Labeler - LANGE SAS (275956105) Registrant - LANGE SAS (275956105) Establishment Name Address ID/FEI Business Operations LANGE SAS 275956105 manufacture(51830-020)