NDC 68807-320 Cellular Radiance Emulsion Spf 30 La Prairie
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What is NDC 68807-320?
What are the uses for Cellular Radiance Emulsion Spf 30 La Prairie?
Which are Cellular Radiance Emulsion Spf 30 La Prairie 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)
Which are Cellular Radiance Emulsion Spf 30 La Prairie 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DOCOSANOL (UNII: 9G1OE216XY)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BATILOL (UNII: 39YR661C4U)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- SALICORNIA EUROPAEA (UNII: 6ADL50JAKW)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ALPINIA GALANGA LEAF (UNII: GD58MI8TU5)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PAPAYA (UNII: KU94FIY6JB)
- CHOLESTERYL NONANOATE (UNII: 4313O7P4XW)
- BLACK COHOSH (UNII: K73E24S6X9)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828)
- COPPER GLUCONATE (UNII: RV823G6G67)
- ACTINIDIA POLYGAMA FRUIT (UNII: CJA97047JF)
- GOLD (UNII: 79Y1949PYO)
- CHOLESTERYL OLEATE (UNII: 3DPK9KFN2M)
- CORALLINA OFFICINALIS (UNII: 4004498D06)
- CARBOMER 934 (UNII: Z135WT9208)
- CHOLESTERYL STEARATE (UNII: I1Q82N9DYQ)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- PHORMIDIUM PERSICINUM (UNII: ZA983U4810)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DEXTRAN 1 (UNII: I8LHQ0D645)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- GERANIOL (UNII: L837108USY)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
- EUGENOL (UNII: 3T8H1794QW)
- BENZYL SALICYLATE (UNII: WAO5MNK9TU)
- LIMONENE, (-)- (UNII: 47MAJ1Y2NE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SORBIC ACID (UNII: X045WJ989B)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
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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".