NDC 11697-319 Aloe Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 11697-319?
What are the uses for Aloe Sunscreen?
Which are Aloe Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Aloe 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:
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- WATER (UNII: 059QF0KO0R)
- PROPANEDIOL (UNII: 5965N8W85T)
- DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- POLYESTER-7 (UNII: 0841698D2F)
- STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- CETEARETH-25 (UNII: 8FA93U5T67)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DISODIUM ETHYLENE DICOCAMIDE PEG-15 DISULFATE (UNII: QI9A6U005W)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- TROLAMINE (UNII: 9O3K93S3TK)
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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".