NDC 33992-7995 Assured 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:
33992-7995
Proprietary Name:
Assured Vaporizing Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
33992
Start Marketing Date: [9]
07-06-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 33992-7995?

The NDC code 33992-7995 is assigned by the FDA to the product Assured Vaporizing Chest Rub which is product labeled by Greenbrier International, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 33992-7995-4 113 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 Assured Vaporizing Chest Rub?

See important warnings under "When using this product"adults and children 2 years and over:rub a thick layer on chest and throat or rub on sore aching musclescover with a warm, dry cloth if desiredkeep clothing loose about throat/chest to help vapors reach the nose/mouthrepeat up to three times per 24hours or as directed by doctorchildren under 2 years do not use.

Which are Assured Vaporizing Chest Rub UNII Codes?

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

Which are Assured Vaporizing Chest Rub 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 Assured 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: 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.

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".