NDC 37012-815 Shopko Anti-wrinkle And Firming Moisturizer Day Broad Spectrum Spf18
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37012 - Shopko Stores Operating Co., Llc
- 37012-815 - Shopko Anti-wrinkle And Firming Moisturizer Day Broad Spectrum Spf18
Product Packages
NDC Code 37012-815-12
Package Description: 1 JAR in 1 CARTON / 48 g in 1 JAR
Product Details
What is NDC 37012-815?
What are the uses for Shopko Anti-wrinkle And Firming Moisturizer Day Broad Spectrum Spf18?
Which are Shopko Anti-wrinkle And Firming Moisturizer Day Broad Spectrum Spf18 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 Anti-wrinkle And Firming Moisturizer Day Broad Spectrum Spf18 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)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- GLYCERIN (UNII: PDC6A3C0OX)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- ROYAL JELLY (UNII: L497I37F0C)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- PALMITIC ACID (UNII: 2V16EO95H1)
- POLYGLYCERYL-10 STEARATE (UNII: 90TF85HH91)
- DOCOSANOL (UNII: 9G1OE216XY)
- SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PALMITOYL TETRAPEPTIDE-7 (UNII: Q41S464P1R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- TROLAMINE (UNII: 9O3K93S3TK)
- SOY PROTEIN (UNII: R44IWB3RN5)
- XANTHAN GUM (UNII: TTV12P4NEE)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PEG-20 STEARATE (UNII: NBX892EA57)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ALCOHOL (UNII: 3K9958V90M)
* 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".