NDC 14783-129 Lbel Dermo Clarite Brightening And Moisturizing Facial Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 14783 - Ventura International Ltd
- 14783-129 - Lbel Dermo Clarite Brightening And Moisturizing Facial Spf 30
Product Packages
NDC Code 14783-129-01
Package Description: 1 JAR in 1 BOX / 30 mL in 1 JAR
Product Details
What is NDC 14783-129?
What are the uses for Lbel Dermo Clarite Brightening And Moisturizing Facial Spf 30?
Which are Lbel Dermo Clarite Brightening And Moisturizing Facial Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Lbel Dermo Clarite Brightening And Moisturizing Facial Spf 30 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
- HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- XANTHAN GUM (UNII: TTV12P4NEE)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIMETHYLMETHOXY CHROMANYL PALMITATE (UNII: 5G222ZDK7U)
- CETEARYL ISONONANOATE (UNII: P5O01U99NI)
- SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)
- ACACIA (UNII: 5C5403N26O)
- EDETATE SODIUM (UNII: MP1J8420LU)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CETEARETH-12 (UNII: 7V4MR24V5P)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STANNIC OXIDE (UNII: KM7N50LOS6)
* 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".