NDC 72667-003 Drive Sunscreen Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72667 - Inspec Solutions Llc.
- 72667-003 - Drive Sunscreen Spf 50
Product Packages
NDC Code 72667-003-01
Package Description: 177 mL in 1 CAN
NDC Code 72667-003-02
Package Description: 89 mL in 1 CAN
NDC Code 72667-003-03
Package Description: 30 mL in 1 CAN
Product Details
What is NDC 72667-003?
What are the uses for Drive Sunscreen Spf 50?
Which are Drive Sunscreen Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- 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 Drive Sunscreen 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:
- RETINYL RETINOATE (UNII: 5AT5X9J439)
- 1,2,3,4,5,6,7,8-OCTAHYDRO-8,8-DIMETHYL-2-NAPHTHALENECARBONITRILE (UNII: EB12VHM8TR)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- TOCOPHEROL (UNII: R0ZB2556P8)
- STEAROXYTRIMETHYLSILANE (UNII: 9862TW94B2)
- BEHENYL BEHENATE (UNII: K8NU647RJ0)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)
- ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)
- GLYCERIN (UNII: PDC6A3C0OX)
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[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".