NDC 71425-010 Glossier Invisible Shield Daily Sunscreen Broad Spectrum Spf 35
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71425 - Glossier Inc.
- 71425-010 - Glossier Invisible Shield Daily Sunscreen Broad Spectrum Spf 35
Product Packages
NDC Code 71425-010-30
Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE
Product Details
What is NDC 71425-010?
What are the uses for Glossier Invisible Shield Daily Sunscreen Broad Spectrum Spf 35?
Which are Glossier Invisible Shield Daily Sunscreen Broad Spectrum Spf 35 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)
Which are Glossier Invisible Shield Daily Sunscreen Broad Spectrum Spf 35 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- METHYL TRIMETHICONE (UNII: S73ZQI0GXM)
- BIOSACCHARIDE GUM-4 (UNII: 9XRL057X90)
- CAPRYLYL TRIMETHICONE (UNII: H6HK6E4EB1)
- PROPANEDIOL (UNII: 5965N8W85T)
- BIS-ETHYLHEXYL HYDROXYDIMETHOXY BENZYLMALONATE (UNII: 7D4Q5YJ8NV)
- BETAINE (UNII: 3SCV180C9W)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW) (UNII: J2S07SB0YL)
- DIBUTYL LAUROYL GLUTAMIDE (UNII: 3V7K3IA58X)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- HIPPOPHAE RHAMNOIDES FRUIT (UNII: AVL0R9111T)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- CITRUS BIOFLAVONOIDS (UNII: BD70459I50)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
- BRASSICA OLERACEA VAR. BOTRYTIS WHOLE (UNII: 87M72T7VW1)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
* 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".