NDC 58443-0169 California Tan Spf 15 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58443 - Prime Enterprises Inc.
- 58443-0169 - California Tan
Product Characteristics
Product Packages
NDC Code 58443-0169-4
Package Description: 133 mL in 1 TUBE
Product Details
What is NDC 58443-0169?
What are the uses for California Tan Spf 15 Sunscreen?
Which are California Tan Spf 15 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 California Tan Spf 15 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:
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PYRUVIC ACID (UNII: 8558G7RUTR)
- AMINO ACIDS (UNII: 0O72R8RF8A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- MICROCOCCUS LUTEUS (UNII: LV6L29Z6AX)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DEXTROSE (UNII: IY9XDZ35W2)
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- N-BUTYLPHTHALIMIDE (UNII: 5TH1DKT35E)
- COLEUS FORSKOHLII ROOT OIL (UNII: 5NXR7DJ9WO)
- SOY PROTEIN (UNII: R44IWB3RN5)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- WATER (UNII: 059QF0KO0R)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
* 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".