NDC 13630-0060 Solmate Broad Spectrum Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13630 - Prime Packaging, Inc.
- 13630-0060 - Solmate
Product Characteristics
Product Packages
NDC Code 13630-0060-4
Package Description: 177 mL in 1 CAN
Product Details
What is NDC 13630-0060?
What are the uses for Solmate Broad Spectrum Spf 50?
Which are Solmate Broad Spectrum Spf 50 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 Solmate Broad Spectrum Spf 50 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 (UNII: 71DD5V995L)
- BUTYL ACRYLATE/C16-C20 ALKYL METHACRYLATE/METHACRYLIC ACID/METHYL METHACRYLATE COPOLYMER (UNII: 7K68DGG29P)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- 3-BUTYLPHTHALIDE (UNII: 822Q956KGM)
- ISOPROPYLPHTHALIMIDE (UNII: 1J1MM83329)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CHAMOMILE (UNII: FGL3685T2X)
- WATER (UNII: 059QF0KO0R)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SORBITOL (UNII: 506T60A25R)
- BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
* 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".