NDC 58443-0096 California Tan Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 58443-0096?
What are the uses for California Tan Broad Spectrum Spf 30?
Which are California Tan 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)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are California Tan 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:
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COLEUS FORSKOHLII ROOT OIL (UNII: 5NXR7DJ9WO)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLUCOSE OXIDASE (UNII: 0T8392U5N1)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- SOY PROTEIN (UNII: R44IWB3RN5)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- N,N-DIMETHYL-2-OCTADECANAMINE (UNII: C358MC5735)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- CATALASE (MICROCOCCUS LUTEUS) (UNII: 7TXA8K9WAE)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- AMINO ACIDS (UNII: 0O72R8RF8A)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PYRUVIC ACID (UNII: 8558G7RUTR)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- CALCIUM (UNII: SY7Q814VUP)
- MAGNESIUM (UNII: I38ZP9992A)
- ZINC (UNII: J41CSQ7QDS)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STYRENE (UNII: 44LJ2U959V)
* 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".