NDC 76168-308 Maximum Strength Lidocaine Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76168 - Velocity Pharma Llc
- 76168-308 - Maximum Strength Lidocaine Patch
Product Packages
NDC Code 76168-308-13
Package Description: 6 POUCH in 1 CARTON / 1 PATCH in 1 POUCH
Product Details
What is NDC 76168-308?
What are the uses for Maximum Strength Lidocaine Patch?
Which are Maximum Strength Lidocaine Patch UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
Which are Maximum Strength Lidocaine Patch 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:
- SODIUM ALUMINIUM SILICATE (UNII: 058TS43PSM)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MINERAL OIL (UNII: T5L8T28FGP)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
- STYRENE (UNII: 44LJ2U959V)
- POLYBUTESTER (UNII: A68634Y1LL)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Maximum Strength Lidocaine Patch?
- RxCUI: 1737778 - lidocaine 4 % Medicated Patch
- RxCUI: 1737778 - lidocaine 0.04 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".