NDC 10157-9608 Blistex Medicated Mint Lip Balm
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10157 - Blistex Inc.
- 10157-9608 - Blistex
Product Characteristics
Product Packages
NDC Code 10157-9608-3
Package Description: 3 CYLINDER in 1 BLISTER PACK / 4.25 g in 1 CYLINDER (10157-9608-1)
Product Details
What is NDC 10157-9608?
What are the uses for Blistex Medicated Mint Lip Balm?
Which are Blistex Medicated Mint Lip Balm UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- PADIMATE O (UNII: Z11006CMUZ)
- PADIMATE O (UNII: Z11006CMUZ) (Active Moiety)
Which are Blistex Medicated Mint Lip Balm 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)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- CANDELILLA WAX (UNII: WL0328HX19)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
- ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
- LANOLIN (UNII: 7EV65EAW6H)
- LANOLIN OIL (UNII: OVV5IIJ58F)
- MENTHOL (UNII: L7T10EIP3A)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- MINERAL OIL (UNII: T5L8T28FGP)
- PARAFFIN (UNII: I9O0E3H2ZE)
- PETROLATUM (UNII: 4T6H12BN9U)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- D&C RED NO. 6 (UNII: 481744AI4O)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- COCOA BUTTER (UNII: 512OYT1CRR)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* 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".