NDC 76150-333 Habit Spf 38 Cucumber Mister
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 76150-333?
What are the uses for Habit Spf 38 Cucumber Mister?
Which are Habit Spf 38 Cucumber Mister UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Habit Spf 38 Cucumber Mister 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:
- DICAPRYL SUCCINATE (UNII: 8XD1ZF2M1M)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- DICAPRYLYL ETHER (UNII: 77JZM5516Z)
- LEVOMENOL (UNII: 24WE03BX2T)
- ETHYL FERULATE (UNII: 5B8915UELW)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- ALCOHOL (UNII: 3K9958V90M)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- CUCUMBER (UNII: YY7C30VXJT)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
* 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".