NDC 68807-304 Anti-aging Emulsion Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68807-304?
What are the uses for Anti-aging Emulsion Spf 30?
Which are Anti-aging Emulsion Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Anti-aging Emulsion Spf 30 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PANAX GINSENG ROOT WATER (UNII: P9T4K47OM0)
- EQUISETUM ARVENSE TOP (UNII: 1DP6Y6B65Z)
- URSOLIC ACID (UNII: P3M2575F3F)
- CAPRYLIC/CAPRIC ACID (UNII: DI775RT244)
- ACACIA (UNII: 5C5403N26O)
- SERINE (UNII: 452VLY9402)
- CARNOSINE (UNII: 8HO6PVN24W)
- BANCHA TEA LEAF/TWIG (UNII: EWI42IEH1C)
- SOYBEAN OIL (UNII: 241ATL177A)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MILK THISTLE (UNII: U946SH95EE)
- ECHIUM PLANTAGINEUM SEED OIL (UNII: PIB7XBU8XW)
- SUCROSE (UNII: C151H8M554)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- POLYISOBUTYLENE (35000 MW) (UNII: 98553S1MHQ)
- CARBOMER 934 (UNII: Z135WT9208)
- MICA (UNII: V8A1AW0880)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- GERANIOL (UNII: L837108USY)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- CITRONELLAL (UNII: QB99VZZ7GZ)
- EUGENOL (UNII: 3T8H1794QW)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
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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".