NDC 69695-1974 Flexin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69695 - Whyteman Labs Llc
- 69695-1974 - Flexin
Product Packages
NDC Code 69695-1974-1
Package Description: 15 POUCH in 1 BOX / 5 PATCH in 1 POUCH
Product Details
What is NDC 69695-1974?
What are the uses for Flexin?
Which are Flexin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Flexin 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:
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- EDETIC ACID (UNII: 9G34HU7RV0)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
What is the NDC to RxNorm Crosswalk for Flexin?
- RxCUI: 1300889 - capsaicin 0.0375 % / menthol 5 % Medicated Patch
- RxCUI: 1300889 - capsaicin 0.000375 MG/MG / menthol 0.05 MG/MG Medicated Patch
* 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".