NDC 20151-056 Purifying Oxygenating Serum
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 20151 - Casmara Cosmetics, Sa
- 20151-056 - Purifying Oxygenating Serum
Product Packages
NDC Code 20151-056-02
Package Description: 1 BOTTLE, DISPENSING in 1 CARTON / 50 mL in 1 BOTTLE, DISPENSING (20151-056-01)
Product Details
What is NDC 20151-056?
What are the uses for Purifying Oxygenating Serum?
Which are Purifying Oxygenating Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Purifying Oxygenating Serum 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:
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- CERAMIDE NS DILAURATE (UNII: 1SL625KAAV)
- SUCROSE PALMITATE (UNII: 3OSQ643ZK5)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PEG-40 CASTOR OIL (UNII: 4ERD2076EF)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- BETAINE (UNII: 3SCV180C9W)
- DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- RIBOSE, D- (UNII: 681HV46001)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)
- PERFLUNAFENE (UNII: 54A06VV62N)
- SIMMONDSIA CHINENSIS SEED (UNII: D24K2Q1F6H)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
* 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".