NDC 61543-3130 Pain Bust R Ii

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:
61543-3130
Proprietary Name:
Pain Bust R Ii
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cca Industries, Inc.
Labeler Code:
61543
Start Marketing Date: [9]
12-23-2011
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 61543-3130-3

Package Description: 1 JAR in 1 CARTON / 85 g in 1 JAR

Product Details

What is NDC 61543-3130?

The NDC code 61543-3130 is assigned by the FDA to the product Pain Bust R Ii which is product labeled by Cca Industries, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61543-3130-3 1 jar in 1 carton / 85 g in 1 jar. 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 Bust R Ii?

Adults and children over 17 yearsapply generously to affected area; massage into painful area until thoroughly absorbed into skin; repeat as necessary but no more than 4 times dailychildren 17 years or youngerdo not use without asking a doctor

Which are Pain Bust R Ii UNII Codes?

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

Which are Pain Bust R Ii 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 Bust R Ii?

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: 259102 - menthol 12 % / methyl salicylate 17 % Topical Cream
  • RxCUI: 259102 - menthol 120 MG/ML / methyl salicylate 170 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".