NDC 76168-067 Maximum Strength Lidocaine Patch
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76168-067?
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:
- ALGELDRATE (UNII: 03J11K103C)
- BENTONITE (UNII: A3N5ZCN45C)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- OLEIC ACID (UNII: 2UMI9U37CP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BORATE (UNII: 91MBZ8H3QO)
- TROLAMINE (UNII: 9O3K93S3TK)
- TARTARIC ACID (UNII: W4888I119H)
- UREA (UNII: 8W8T17847W)
- WATER (UNII: 059QF0KO0R)
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".