NDC 82160-672 Derma Charcoal Mask
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 82160 - Pella Pharmaceuticals Co .ltd
- 82160-672 - Derma Charcoal Mask
Product Characteristics
Product Packages
NDC Code 82160-672-01
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 75 g in 1 TUBE, WITH APPLICATOR
Product Details
What is NDC 82160-672?
What are the uses for Derma Charcoal Mask?
Which are Derma Charcoal Mask UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)
- ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (Active Moiety)
- JOJOBA OIL (UNII: 724GKU717M)
- JOJOBA OIL (UNII: 724GKU717M) (Active Moiety)
- DEXPANTHENOL (UNII: 1O6C93RI7Z)
- DEXPANTHENOL (UNII: 1O6C93RI7Z) (Active Moiety)
Which are Derma Charcoal Mask 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:
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- WATER (UNII: 059QF0KO0R)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- ALCOHOL (UNII: 3K9958V90M)
- KAOLIN (UNII: 24H4NWX5CO)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WHITE WAX (UNII: 7G1J5DA97F)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCERIN (UNII: PDC6A3C0OX)
* 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".