NDC 68807-326 Line Interception Power Duo Day Cream Suncreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68807-326?
What are the uses for Line Interception Power Duo Day Cream Suncreen Broad Spectrum Spf 30?
Which are Line Interception Power Duo 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 Line Interception Power Duo 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".