NDC 11559-065 Revitalizing Supreme Youth Power Creme Broad Spectrum Spf 25
Avobenzone, Homosalate, Octisalate,And Octocrylene Cream Topical - View Dosage, Usage, Ingredients, Routes, UNII
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Code Structure Chart
Product Details
What is NDC 11559-065?
What are the uses for Revitalizing Supreme Youth Power Creme Broad Spectrum Spf 25?
What are Revitalizing Supreme Youth Power Creme Broad Spectrum Spf 25 Active Ingredients?
Which are Revitalizing Supreme Youth Power Creme Broad Spectrum Spf 25 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 Revitalizing Supreme Youth Power Creme Broad Spectrum Spf 25 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:
- SUCROSE (UNII: C151H8M554)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SIGESBECKIA ORIENTALIS FLOWERING TOP (UNII: 6UL878YAR7)
- HEPTYL UNDECYLENATE (UNII: W77QUB6GXO)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATERMELON (UNII: 231473QB6R)
- HORDEUM VULGARE WHOLE (UNII: 8JBE478M5Q)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- SILYBUM MARIANUM SEED (UNII: U946SH95EE)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- STEARETH-21 (UNII: 53J3F32P58)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- TRISILOXANE (UNII: 9G1ZW13R0G)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- LENS CULINARIS FRUIT (UNII: ZYZ076G9JH)
- SORBITOL (UNII: 506T60A25R)
- C13-15 ALKANE (UNII: 114P5I43UJ)
- FD&C RED NO. 4 (UNII: X3W0AM1JLX)
- ISOCETETH-20 (UNII: O020065R7Z)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
- HIBISCUS MUTABILIS FLOWER (UNII: 2O22799NBH)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- OPUNTIA TUNA FLOWERING TOP (UNII: R4AS8333O2)
- PORPHYRIDIUM PURPUREUM (UNII: K2P8K2558N)
- CUCUMBER (UNII: YY7C30VXJT)
- DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- WHEY (UNII: 8617Z5FMF6)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LAMINARIA DIGITATA (UNII: 15E7C67EE8)
- APPLE (UNII: B423VGH5S9)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- PEG-100 STEARATE (UNII: YD01N1999R)
- MORINGA OLEIFERA SEED (UNII: TIX5482832)
- METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
- CAFFEINE (UNII: 3G6A5W338E)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- PROPYLENE GLYCOL DICAPRATE (UNII: U783H9JHWY)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- MYRISTYL LAURATE (UNII: 58U0NZN2BT)
- DIBUTYL ADIPATE (UNII: F4K100DXP3)
- BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
- WATER (UNII: 059QF0KO0R)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- VINYLPYRROLIDONE/EICOSENE COPOLYMER (UNII: 035MV9S1C3)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- NARCISSUS TAZETTA BULB (UNII: K17762966S)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".