NDC 10157-9865 Blistex Enhancement Series (deep Renewal And Silk And Shine)
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 10157-9865?
What are the uses for Blistex Enhancement Series (deep Renewal And Silk And Shine)?
Which are Blistex Enhancement Series (deep Renewal And Silk And Shine) UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Blistex Enhancement Series (deep Renewal And Silk And Shine) 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:
- YELLOW WAX (UNII: 2ZA36H0S2V)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- PETROLATUM (UNII: 4T6H12BN9U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)
- CASTOR OIL (UNII: D5340Y2I9G)
- SACCHARIN (UNII: FST467XS7D)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SORBIC ACID (UNII: X045WJ989B)
- SQUALANE (UNII: GW89575KF9)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- CHONDROITIN SULFATE SODIUM (SHARK) (UNII: Q75WVO004L)
- UBIDECARENONE (UNII: EJ27X76M46)
- SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- DOCOSANOL (UNII: 9G1OE216XY)
- MICA (UNII: V8A1AW0880)
- MINERAL OIL (UNII: T5L8T28FGP)
- PANTHENYL ETHYL ETHER (UNII: F4WMF8NX3B)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SANDALWOOD (UNII: 3641YW25N2)
- CERESIN (UNII: Q1LS2UJO3A)
* 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".