NDC 10157-9858 Blistex Enhancement Series
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 10157-9858?
What are the uses for Blistex Enhancement Series?
Which are Blistex Enhancement Series 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 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:
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- CERESIN (UNII: Q1LS2UJO3A)
- PARAFFIN (UNII: I9O0E3H2ZE)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- DOCOSANOL (UNII: 9G1OE216XY)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- SHEA BUTTER (UNII: K49155WL9Y)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- D&C RED NO. 6 (UNII: 481744AI4O)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MICA (UNII: V8A1AW0880)
- PANTHENYL ETHYL ETHER (UNII: F4WMF8NX3B)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- CASTOR OIL (UNII: D5340Y2I9G)
- SANDALWOOD (UNII: 3641YW25N2)
- SACCHARIN (UNII: FST467XS7D)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- DIPALMITOYL HYDROXYPROLINE (UNII: E6AHA53N1H)
- LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PENTAERYTHRITYL TETRAISOSTEARATE (UNII: 9D7IK5483F)
- POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)
- SORBIC ACID (UNII: X045WJ989B)
- SQUALANE (UNII: GW89575KF9)
- TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
- MARINE COLLAGEN, SOLUBLE (UNII: 8JC99XGU4W)
- CHONDROITIN SULFATE SODIUM (SHARK) (UNII: Q75WVO004L)
- UBIDECARENONE (UNII: EJ27X76M46)
- SIMMONDSIA CHINENSIS SEED WAX (UNII: 47X6Y9FJJ2)
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[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".