NDC 51452-173 Point Relief Lidospot
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 51452-173?
What are the uses for Point Relief Lidospot?
Which are Point Relief Lidospot UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Point Relief Lidospot 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:
- KAOLIN (UNII: 24H4NWX5CO)
- TARTARIC ACID (UNII: W4888I119H)
- WATER (UNII: 059QF0KO0R)
- DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- GLYCERIN (UNII: PDC6A3C0OX)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- POVIDONE K90 (UNII: RDH86HJV5Z)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
What is the NDC to RxNorm Crosswalk for Point Relief Lidospot?
- 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".