NDC 69159-003 Lidocaine Patch
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69159 - Foshan Aqua Gel Biotech Co., Ltd.,
- 69159-003 - Lidocaine Patch
Product Packages
NDC Code 69159-003-01
Package Description: 300 PATCH in 1 CASE / 1 PATCH in 1 PATCH
Product Details
What is NDC 69159-003?
What are the uses for Lidocaine Patch?
Which are 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 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 POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- KAOLIN (UNII: 24H4NWX5CO)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- POVIDONE (UNII: FZ989GH94E)
- DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
- GLYCEROL (1-(12-HYDROXYSTEARATE)) (UNII: X84XWP4TOC)
- POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
- TARTARIC ACID (UNII: W4888I119H)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Lidocaine Patch?
- RxCUI: 1737778 - lidocaine 4 % Medicated Patch
- RxCUI: 1737778 - lidocaine 0.04 MG/MG Medicated Patch
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Patient Education
Lidocaine Transdermal Patch
Prescription lidocaine transdermal (Dermalid, Lidoderm, Ztildo) is used to relieve the pain of post-herpetic neuralgia (PHN; burning, stabbing pains, or aches that may last for months or years after a shingles infection). Nonprescription (over-the-counter) lidocaine (Absorbine Jr, Aspercreme, Lidocare, Salonpas, others) is also available to relieve minor pain in shoulders, arms, neck and legs in adults and children 12 years of age and older. Lidocaine is in a class of medications called local anesthetics. It works by stopping nerves from sending pain signals.
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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".