NDC 53407-104 Algenist
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53407 - Solazyme, Inc.
- 53407-104 - Algenist
Product Packages
NDC Code 53407-104-60
Package Description: 1 CARTON in 1 BOX / 1 JAR in 1 CARTON / 60 mL in 1 JAR
Product Details
What is NDC 53407-104?
What are the uses for Algenist?
Which are Algenist UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Algenist 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- SHEA BUTTER (UNII: K49155WL9Y)
- DI-C12-15 ALKYL FUMARATE (UNII: A1CB3Z898P)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- APPLE (UNII: B423VGH5S9)
- TETRAPEPTIDE-21 (UNII: 179JUC43HU)
- ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)
- ALARIA ESCULENTA (UNII: EJ9JK8J58D)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
- BIOTIN (UNII: 6SO6U10H04)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- XANTHAN GUM (UNII: TTV12P4NEE)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- MANNITOL (UNII: 3OWL53L36A)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
* 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".