NDC 69512-001 Alivio Medicated Pain
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69512 - Alivio Medical Products, Llc
- 69512-001 - Alivio Medicated Pain
Product Packages
NDC Code 69512-001-01
Package Description: 15 PATCH in 1 BOX / 8.5 g in 1 PATCH
Product Details
What is NDC 69512-001?
What are the uses for Alivio Medicated Pain?
Which are Alivio Medicated Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
Which are Alivio Medicated Pain 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:
- ACRYLIC ACID (UNII: J94PBK7X8S)
- ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- 2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- METHYL ACRYLATE (UNII: WC487PR91H)
- NONOXYNOL-30 (UNII: JJX07DG188)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TALC (UNII: 7SEV7J4R1U)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Alivio Medicated Pain?
- RxCUI: 1599652 - capsaicin 0.03 % / menthol 5 % Medicated Patch
- RxCUI: 1599652 - capsaicin 0.0003 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".