NDC 55629-060 Maximum Strength Lidocaine Patch

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55629-060
Proprietary Name:
Maximum Strength Lidocaine Patch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
One2zee Limited Liability Company
Labeler Code:
55629
Start Marketing Date: [9]
01-21-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
RECTANGLE (C48347)

Product Packages

NDC Code 55629-060-02

Package Description: 20 POUCH in 1 BOX / 1 PATCH in 1 POUCH (55629-060-01)

NDC Code 55629-060-03

Package Description: 45 POUCH in 1 BOX / 1 PATCH in 1 POUCH (55629-060-01)

Product Details

What is NDC 55629-060?

The NDC code 55629-060 is assigned by the FDA to the product Maximum Strength Lidocaine Patch which is product labeled by One2zee Limited Liability Company. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 55629-060-02 20 pouch in 1 box / 1 patch in 1 pouch (55629-060-01), 55629-060-03 45 pouch in 1 box / 1 patch in 1 pouch (55629-060-01). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Maximum Strength Lidocaine Patch?

Adults and children over 12 years:clean and dry affected arearemove backing from patch by firmly grasping both ends and gently pulling until backing separates in middlecarefully remove smaller portion of backing from patch and apply exposed portion of patch to affected areaonce exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected areause 1 patch for up to 12 hourschildren 12 years or younger: ask a doctor

Which are Maximum Strength Lidocaine Patch UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Maximum Strength Lidocaine Patch?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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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Product Footnotes

[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".