NDC 43493-0002 Pain Relieving Iampur

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:
43493-0002
Proprietary Name:
Pain Relieving Iampur
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Avaria Health & Beauty Corp
Labeler Code:
43493
Start Marketing Date: [9]
05-24-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 43493-0002-4

Package Description: 120 g in 1 VIAL, PLASTIC

Product Details

What is NDC 43493-0002?

The NDC code 43493-0002 is assigned by the FDA to the product Pain Relieving Iampur which is product labeled by Avaria Health & Beauty Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 43493-0002-4 120 g in 1 vial, plastic . 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 Relieving Iampur?

UsesTemporarily relieves minor muscle pain, joint pain.  Temporarily relieves pain associated with:  arthritis pain, backache, strains, sprains, and bruises.

Which are Pain Relieving Iampur UNII Codes?

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

Which are Pain Relieving Iampur 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 Relieving Iampur?

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: 1368275 - camphor 4 % / menthol 4 % / methyl salicylate 11 % Topical Cream
  • RxCUI: 1368275 - camphor 40 MG/ML / menthol 40 MG/ML / methyl salicylate 110 MG/ML Topical Cream
  • RxCUI: 1425861 - Iampur Camphor 4 % / Menthol 4 % / methyl salicylate 11 % Topical Cream
  • RxCUI: 1425861 - camphor 40 MG/ML / menthol 40 MG/ML / methyl salicylate 110 MG/ML Topical Cream [Iampur]

* 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".