NDC 50682-527 Lidopatch Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50682 - 3t Federal Solutions Llc
- 50682-527 - Lidopatch
Product Packages
NDC Code 50682-527-03
Package Description: 3 POUCH in 1 CARTON / 1 PATCH in 1 POUCH
NDC Code 50682-527-07
Package Description: 7 POUCH in 1 CARTON / 1 PATCH in 1 POUCH
NDC Code 50682-527-30
Package Description: 30 POUCH in 1 CARTON / 1 PATCH in 1 POUCH
Product Details
What is NDC 50682-527?
What are the uses for Lidopatch Pain Relief?
Which are Lidopatch Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Lidopatch Pain Relief 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- ACRYLAMIDE (UNII: 20R035KLCI)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- UREA (UNII: 8W8T17847W)
What is the NDC to RxNorm Crosswalk for Lidopatch Pain Relief?
- RxCUI: 1249758 - lidocaine 4 % / menthol 1 % Medicated Patch
- RxCUI: 1249758 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch
- RxCUI: 1249763 - LidoPatch 4 % / 1 % Medicated Patch
- RxCUI: 1249763 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch [Lidopatch]
- RxCUI: 1249763 - LidoPatch (lidocaine 4 % / menthol 1 % ) Medicated Patch
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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".