NDC 36800-042 Pain Relief Rub

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:
36800-042
Proprietary Name:
Pain Relief Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Topco Associates Llc
Labeler Code:
36800
Start Marketing Date: [9]
09-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 36800-042-04

Package Description: 1 TUBE in 1 BOX / 114 g in 1 TUBE

Product Details

What is NDC 36800-042?

The NDC code 36800-042 is assigned by the FDA to the product Pain Relief Rub which is product labeled by Topco Associates Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 36800-042-04 1 tube in 1 box / 114 g in 1 tube. 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 Pain Relief Rub?

Use only as directedadults and children 12 years of age and older:             apply to affected area not more than 3 to 4 times dailychildren under 12 years of age:  ask a doctor

Which are Pain Relief Rub UNII Codes?

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

Which are Pain Relief Rub 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 Pain Relief Rub?

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: 283083 - camphor 4 % / menthol 10 % / methyl salicylate 30 % Topical Cream
  • RxCUI: 283083 - camphor 40 MG/ML / menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical Cream

* 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".