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  4. NDC Product Code: 76437-609 Reed Therapeutics Pain Relieving Therapy

NDC 76437-609 Reed Therapeutics Pain Relieving Therapy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76437-609?
  4. Reed Therapeutics Pain Relieving Therapy Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76437-609
Proprietary Name:
Reed Therapeutics Pain Relieving Therapy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Reed Therapeutics
Labeler Code:
76437
Product Label ID:
5ee37805-f1c6-467a-bdf2-f67368347e11
Start Marketing Date: [9]
01-09-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76437-609-03

Package Description: 87 g in 1 CANISTER

NDC Code 76437-609-05

Package Description: 150 g in 1 TUBE

NDC Code 76437-609-16

Package Description: 454 g in 1 BOTTLE, PUMP

Product Details

What is NDC 76437-609?

The NDC code 76437-609 is assigned by the FDA to the product Reed Therapeutics Pain Relieving Therapy which is product labeled by Reed Therapeutics. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 76437-609-03 87 g in 1 canister , 76437-609-05 150 g in 1 tube , 76437-609-16 454 g in 1 bottle, pump . 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 Reed Therapeutics Pain Relieving Therapy?

Adults and children 12 year and older: Gently massage and apply to affected area 3-4 times daily. Massage not necesssary but may enhance relief.Children under 12 years of age: consult a physician.

Which are Reed Therapeutics Pain Relieving Therapy UNII Codes?

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

Which are Reed Therapeutics Pain Relieving Therapy 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 Reed Therapeutics Pain Relieving Therapy?

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:
  • RxCUI: 1546102 - camphor 0.2 % / menthol 4 % / methyl salicylate 12.5 % Topical Gel
  • RxCUI: 1546102 - camphor 0.002 MG/MG / menthol 0.04 MG/MG / methyl salicylate 0.125 MG/MG Topical Gel

* Please review the disclaimer below.

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".