NDC 63730-364 Dry Oil Antioxidant Sun Protection
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63730 - Natura Bisse International Sa
- 63730-364 - Dry Oil Antioxidant Sun Protection
Product Packages
NDC Code 63730-364-01
Package Description: 100 g in 1 PACKAGE
Product Details
What is NDC 63730-364?
What are the uses for Dry Oil Antioxidant Sun Protection?
Which are Dry Oil Antioxidant Sun Protection 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)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Dry Oil Antioxidant Sun Protection 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:
- ALCOHOL (UNII: 3K9958V90M)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- BENZOTRIAZOLYL DODECYL P-CRESOL (UNII: 298PX4M11X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- GLYCERYL LINOLEATE (UNII: 4763AXI84L)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- LEVOMENOL (UNII: 24WE03BX2T)
- HELIANTHUS ANNUUS WHOLE (UNII: 17S27ZT6KR)
- CITRUS NOBILIS (UNII: 8MFF77J91V)
- CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)
- GLYCERYL LINOLENATE (UNII: SGB6X4G86K)
- DAUCUS CAROTA SUBSP. SATIVUS WHOLE (UNII: F9I9HZH3O3)
- BETA CAROTENE (UNII: 01YAE03M7J)
- 7-DEHYDROCHOLESTEROL (UNII: BK1IU07GKF)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- LINALOOL, (+)- (UNII: F4VNO44C09)
- .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
- GERANIOL (UNII: L837108USY)
- CITRAL (UNII: T7EU0O9VPP)
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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".