NDC 52069-101 Vaporizing Chest 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:
52069-101
Proprietary Name:
Vaporizing Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nova Petroleum & Chemicals Corporation
Labeler Code:
52069
Start Marketing Date: [9]
03-10-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52069-101-04

Package Description: 110 g in 1 JAR

Product Details

What is NDC 52069-101?

The NDC code 52069-101 is assigned by the FDA to the product Vaporizing Chest Rub which is product labeled by Nova Petroleum & Chemicals Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52069-101-04 110 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 Vaporizing Chest Rub?

See important warnings under “When using this product”Adults and children 2 years and older:Rub a thick layer on chest & throat or rub on sore, aching muscles.Cover with a warm, dry cloth if desired.Keep clothing loose about throat/chest to help vapors reach the nose/mouth. Repeat up to three times per 24 hours or as directed by doctor.Children under 2 years of age: ask a doctor.

Which are Vaporizing Chest Rub UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Vaporizing Chest 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: 1042788 - camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Gel
  • RxCUI: 1042788 - camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 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".