NDC 10157-8015 Blistex Ultra Rich Hydration
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10157 - Blistex Inc.
- 10157-8015 - Blistex
Product Packages
NDC Code 10157-8015-1
Package Description: 1 CYLINDER in 1 BLISTER PACK / 3.69 g in 1 CYLINDER
Product Details
What is NDC 10157-8015?
What are the uses for Blistex Ultra Rich Hydration?
Which are Blistex Ultra Rich Hydration UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Blistex Ultra Rich Hydration 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)
- PENTAERYTHRITYL TETRAETHYLHEXANOATE (UNII: XJ7052W897)
- PETROLATUM (UNII: 4T6H12BN9U)
- PARAFFIN (UNII: I9O0E3H2ZE)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SHEA BUTTER (UNII: K49155WL9Y)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- DOCOSANOL (UNII: 9G1OE216XY)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WHEAT GERM OIL (UNII: 14C97E680P)
- PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- CHAMOMILE (UNII: FGL3685T2X)
- CERESIN (UNII: Q1LS2UJO3A)
- COCOA BUTTER (UNII: 512OYT1CRR)
- SACCHARIN (UNII: FST467XS7D)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
* 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".