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  4. NDC Product Code: 71226-002 Painbloc24 Flexi-stretch Pain Tape

NDC 71226-002 Painbloc24 Flexi-stretch Pain Tape

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71226-002?
  4. Painbloc24 Flexi-stretch Pain Tape Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
71226-002
Proprietary Name:
Painbloc24 Flexi-stretch Pain Tape
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vizuri Health Sciences Llc
Labeler Code:
71226
Product Label ID:
0ec02d2a-0310-40c6-a7d8-f762423f4d08
Start Marketing Date: [9]
06-25-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71226-002-09

Package Description: 10 PATCH in 1 CARTON

NDC Code 71226-002-10

Package Description: 5 PATCH in 1 CANISTER

NDC Code 71226-002-17

Package Description: 10 PATCH in 1 CARTON

Product Details

What is NDC 71226-002?

The NDC code 71226-002 is assigned by the FDA to the product Painbloc24 Flexi-stretch Pain Tape which is product labeled by Vizuri Health Sciences Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 71226-002-09 10 patch in 1 carton , 71226-002-10 5 patch in 1 canister , 71226-002-17 10 patch in 1 carton . 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 Painbloc24 Flexi-stretch Pain Tape?

Adults and Children 12 years and older Clean and dry affected area Trim excessive hair for better adhesion Remove roll from container and remove outer wrap Tear off 1 or 2 strips from roll. See illustration for instructions on removing the backing and applying to skin. Apply no more than 3 strips at a time, no more than 2 times a day Some individuals may not experience pain relief until several minutes or hours after applying Seal remaining roll with resealable tab, return to container and close cap securely Use strip as needed for up to 12 hours. Do not remove when wet or directly after showering or bathing. Allow strip to dry and then remove.Children under 12 years: consult a doctor

Which are Painbloc24 Flexi-stretch Pain Tape UNII Codes?

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

Which are Painbloc24 Flexi-stretch Pain Tape 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 Painbloc24 Flexi-stretch Pain Tape?

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:

* Please review the disclaimer below.

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.
[Learn More]


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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".