NDC 51514-0343 Naked One And Done Cream Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 51514-0343?
What are the uses for Naked One And Done Cream Light?
Which are Naked One And Done Cream Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Naked One And Done Cream Light 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:
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- POLYGLYCERYL-2 MONOISOSTEARATE (UNII: 7B8OE71MQC)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ISOCETETH-10 (UNII: 1K92T9919H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- TETRADIUM RUTICARPUM FRUIT (UNII: Q413WWJ3X9)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SORBIC ACID (UNII: X045WJ989B)
- ISODODECANE (UNII: A8289P68Y2)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)
- WATER (UNII: 059QF0KO0R)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
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[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".