NDC 29500-9033 Vaporizing Chest

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:
29500-9033
Proprietary Name:
Vaporizing Chest
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Personal Care Products
Labeler Code:
29500
Start Marketing Date: [9]
04-01-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 29500-9033-1

Package Description: 113 g in 1 JAR

Product Details

What is NDC 29500-9033?

The NDC code 29500-9033 is assigned by the FDA to the product Vaporizing Chest which is product labeled by Personal Care Products. The product's dosage form is . The product is distributed in a single package with assigned NDC code 29500-9033-1 113 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?

Uses on chest and throat, helps temporarily relieve, decrease, suppress, quiet and alleviate cough as may occur with common cold and minor bronchial irritation.

Which are Vaporizing Chest UNII Codes?

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

Which are Vaporizing Chest 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 Vaporizing Chest?

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: 1042786 - camphor 4.7 % / eucalyptus oil 1 % / menthol 1 % Topical Ointment
  • RxCUI: 1042786 - camphor 0.047 MG/MG / Eucalyptus oil 0.01 MG/MG / menthol 0.01 MG/MG Topical Ointment

* 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".