NDC 14783-434 Lbel Dermo Clarite
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 14783-434?
What are the uses for Lbel Dermo Clarite?
Which are Lbel Dermo Clarite UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- ENSULIZOLE (UNII: 9YQ9DI1W42)
- ENSULIZOLE (UNII: 9YQ9DI1W42) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Lbel Dermo Clarite 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)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- ALCOHOL (UNII: 3K9958V90M)
- PHENETHYL BENZOATE (UNII: 0C143929GK)
- TROLAMINE (UNII: 9O3K93S3TK)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- MOTH BEAN (UNII: H7938ON8E5)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PEG-75 STEARATE (UNII: OT38R0N74H)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- SORBIC ACID (UNII: X045WJ989B)
- CETETH-20 (UNII: I835H2IHHX)
- STEARETH-20 (UNII: L0Q8IK9E08)
* 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".