NDC 13630-0078 California Tan Spf 45 Face Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging, Inc.
- 13630-0078 - California Tan
Product Characteristics
Product Packages
NDC Code 13630-0078-4
Package Description: 142 g in 1 CAN
Product Details
What is NDC 13630-0078?
What are the uses for California Tan Spf 45 Face Sunscreen?
Which are California Tan Spf 45 Face Sunscreen 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 California Tan Spf 45 Face 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:
- (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- BUTANE (UNII: 6LV4FOR43R)
- PROPANE (UNII: T75W9911L6)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ISOSTEARIC ACID (UNII: X33R8U0062)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- MATRICARIA CHAMOMILLA FLOWERING TOP OIL (UNII: SA8AR2W4ER)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- LYCIUM BARBARUM FRUIT (UNII: 930626MWDL)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- CETEARETH-22 (UNII: 28VZG1E234)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- AMINO ACIDS (UNII: 0O72R8RF8A)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- SOY PROTEIN (UNII: R44IWB3RN5)
- CALCIUM (UNII: SY7Q814VUP)
- MAGNESIUM (UNII: I38ZP9992A)
- ZINC (UNII: J41CSQ7QDS)
- COLEUS FORSKOHLII ROOT OIL (UNII: 5NXR7DJ9WO)
- CATALASE (MICROCOCCUS LUTEUS) (UNII: 7TXA8K9WAE)
- DEXTROSE (UNII: IY9XDZ35W2)
- ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N)
- PYRUVIC ACID (UNII: 8558G7RUTR)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE)
- QUATERNIUM-15 (UNII: E40U03LEM0)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- WATER (UNII: 059QF0KO0R)
* 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".