NDC 76168-306 Hot And Cold Lidocaine With Menthol Patch Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76168 - Velocity Pharma Llc
- 76168-306 - Hot And Cold Lidocaine With Menthol Patch
Product Packages
NDC Code 76168-306-05
Package Description: 5 PATCH in 1 BOX
Product Details
What is NDC 76168-306?
What are the uses for Hot And Cold Lidocaine With Menthol Patch Pain Relief?
Which are Hot And Cold Lidocaine With Menthol Patch 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 Hot And Cold Lidocaine With Menthol Patch 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:
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- GLYCERIN (UNII: PDC6A3C0OX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- TARTARIC ACID (UNII: W4888I119H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Hot And Cold Lidocaine With Menthol Patch Pain Relief?
- RxCUI: 1249758 - lidocaine 4 % / menthol 1 % Medicated Patch
- RxCUI: 1249758 - lidocaine 0.04 MG/MG / menthol 0.01 MG/MG 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".