NDC 37012-326 Shopko Illuminating Daily Moisturizer Broad Spectrum Spf15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 37012-326?
What are the uses for Shopko Illuminating Daily Moisturizer Broad Spectrum Spf15 Sunscreen?
Which are Shopko Illuminating Daily Moisturizer Broad Spectrum Spf15 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Shopko Illuminating Daily Moisturizer Broad Spectrum Spf15 Sunscreen 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- STEARETH-2 (UNII: V56DFE46J5)
- GLYCERIN (UNII: PDC6A3C0OX)
- STEARETH-21 (UNII: 53J3F32P58)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- PANTHENOL (UNII: WV9CM0O67Z)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- SOY ISOFLAVONES (UNII: 71B37NR06D)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TROLAMINE (UNII: 9O3K93S3TK)
- ALCOHOL (UNII: 3K9958V90M)
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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".