NDC 10157-9848 Blistex Revive And Restore
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 10157-9848?
What are the uses for Blistex Revive And Restore?
Which are Blistex Revive And Restore 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)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN (UNII: 7EV65EAW6H) (Active Moiety)
Which are Blistex Revive And Restore 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:
- ACER SACCHARUM BARK/SAP (UNII: Z120VL0KAC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- SHEA BUTTER (UNII: K49155WL9Y)
- C10-30 CHOLESTEROL/LANOSTEROL ESTERS (UNII: 137SL7IL0Y)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- MENTHOL (UNII: L7T10EIP3A)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- CASTOR OIL (UNII: D5340Y2I9G)
- SACCHARIN (UNII: FST467XS7D)
- SUGARCANE (UNII: 81H2R5AOH3)
- BILBERRY (UNII: 9P2U39H18W)
- JOJOBA OIL (UNII: 724GKU717M)
- SQUALANE (UNII: GW89575KF9)
- COCOA BUTTER (UNII: 512OYT1CRR)
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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".