NDC 51514-0347 Naked Skin One And Done Dark
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51514 - Autumn Harp Inc.
- 51514-0347 - Naked Skin One And Done Dark
Product Packages
NDC Code 51514-0347-1
Package Description: 40 g in 1 TUBE
Product Details
What is NDC 51514-0347?
What are the uses for Naked Skin One And Done Dark?
Which are Naked Skin One And Done Dark UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Naked Skin One And Done Dark 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYGLYCERYL-2 MONOISOSTEARATE (UNII: 7B8OE71MQC)
- PROPANEDIOL (UNII: 5965N8W85T)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- XANTHAN GUM (UNII: TTV12P4NEE)
- ISOPROPYL TITANIUM TRIISOSTEARATE (UNII: 949E3KBJ1I)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ISODODECANE (UNII: A8289P68Y2)
- LAURYL TRISILOXANE (UNII: 5OHO78HI1D)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARALKONIUM HECTORITE (UNII: OLX698AH5P)
- TETRADIUM RUTICARPUM FRUIT (UNII: Q413WWJ3X9)
- SORBIC ACID (UNII: X045WJ989B)
- CYCLOMETHICONE 4 (UNII: CZ227117JE)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOCETETH-10 (UNII: 1K92T9919H)
- DIMETHICONE (UNII: 92RU3N3Y1O)
* 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".