NDC 68807-325 Anti-wrinkle Day Cream Suncreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 68807-325?
What are the uses for Anti-wrinkle Day Cream Suncreen Broad Spectrum Spf 30?
Which are Anti-wrinkle Day Cream Suncreen Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Anti-wrinkle Day Cream Suncreen Broad Spectrum 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
- GLYCOPROTEIN HORMONES ALPHA CHAIN (UNII: 8YJ68CQ409)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- EQUISETUM ARVENSE BRANCH (UNII: 1L0VKZ185E)
- CARNOSINE (UNII: 8HO6PVN24W)
- LACTIC ACID (UNII: 33X04XA5AT)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- DIPEPTIDE DIAMINOBUTYROYL BENZYLAMIDE DIACETATE (UNII: 38H206R00R)
- UREA (UNII: 8W8T17847W)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- INVERT SUGAR (UNII: ED959S6ACY)
- ALANINE (UNII: OF5P57N2ZX)
- GLYCINE (UNII: TE7660XO1C)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- CREATINE (UNII: MU72812GK0)
- DIGLYCERIN (UNII: 3YC120743U)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- TOCOPHEROL (UNII: R0ZB2556P8)
- LACTOBACILLUS REUTERI (UNII: 9913I24QEE)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DOCOSANOL (UNII: 9G1OE216XY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- C20-22 ALKYL PHOSPHATE (UNII: L4VKP0Y7RP)
- STEARETH-21 (UNII: 53J3F32P58)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- XANTHAN GUM (UNII: TTV12P4NEE)
- LINALOOL, (+/-)- (UNII: D81QY6I88E)
- .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)
- HYDROXYCITRONELLAL (UNII: 8SQ0VA4YUR)
- .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
- GERANIOL (UNII: L837108USY)
- BENZYL BENZOATE (UNII: N863NB338G)
- BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
- PSEUDEVERNIA FURFURACEA (UNII: 49ZMN09Q0K)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
* 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".