NDC 51830-020 Lightening Night Cream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51830-020?
What are the uses for Lightening Night Cream?
Which are Lightening Night Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1)
- ETHYL MACADAMIATE (UNII: ANA2NCS6V1) (Active Moiety)
Which are Lightening Night Cream Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".