NDC 71328-044 Clixit Tinted Blemish Concealer Light
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 71328-044?
What are the uses for Clixit Tinted Blemish Concealer Light?
Which are Clixit Tinted Blemish Concealer Light UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Clixit Tinted Blemish Concealer Light 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)
- BENTONITE (UNII: A3N5ZCN45C)
- CANDELILLA WAX (UNII: WL0328HX19)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- RUBUS CHAMAEMORUS SEED OIL (UNII: WH495F04LZ)
- STEARETH-20 (UNII: L0Q8IK9E08)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ZINC OXIDE (UNII: SOI2LOH54Z)
What is the NDC to RxNorm Crosswalk for Clixit Tinted Blemish Concealer Light?
- RxCUI: 247817 - sulfur 4 % Topical Cream
- RxCUI: 247817 - sulfur 40 MG/ML Topical Cream
* 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".