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  4. NDC Product Code: 37205-356 Medicated Chest

NDC 37205-356 Medicated Chest

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 37205-356?
  4. Medicated Chest Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk
  8. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
37205-356
Proprietary Name:
Medicated Chest
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cardinal Health
Labeler Code:
37205
Product Label ID:
5cc11746-eb08-4d60-b7b1-9e723a9e60c6
Start Marketing Date: [9]
01-23-2011
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 37205-356?

The NDC code 37205-356 is assigned by the FDA to the product Medicated Chest which is product labeled by Cardinal Health. The product's dosage form is . The product is distributed in a single package with assigned NDC code 37205-356-56 .05 kg 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 Medicated Chest?

Uses•on chest + throat, temporarily relieves cough due to the common cold•on muscles and joints, temporarily relieves minor aces and pains

Which are Medicated Chest UNII Codes?

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

Which are Medicated 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 Medicated 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: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
  • RxCUI: 727137 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest Rub
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Stick

* Please review the disclaimer below.

Patient Education

Eucalyptus


What is it? Eucalyptus is a tree. Its leaves and oil have been consumed, chewed, and applied to the skin for many conditions.

Eucalyptus contains many different chemicals. These chemicals might have various effects in the body. Also, some research suggests that eucalyptus may have activity against bacteria and fungi.

People use eucalyptus for many conditions including asthma, bronchitis, flu (influenza), and many others, but there is no good scientific evidence to support these uses.
[Learn More]


* 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".