NDC 41499-122 Amar 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:
41499-122
Proprietary Name:
Amar Vaporizing Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
41499
Start Marketing Date: [9]
05-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 41499-122?

The NDC code 41499-122 is assigned by the FDA to the product Amar Vaporizing Chest Rub which is product labeled by Amar Remedies Limited - Mumbai. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41499-122-01 100 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 Amar Vaporizing Chest Rub?

See important warnings under "When using this product"adults and children 2 year and over.rub a thick layer on the throat and chest cough, or rub on sore aching muscles or jointscover with a warm, dry cloth if desiredclothing should be left loose about the throat and chest to help vapors reach the nose and mouthuse up to 3 times daily, or as directed by a doctorchildren under 2 yeas : ask a doctor

Which are Amar Vaporizing Chest Rub UNII Codes?

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

Which are Amar 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 Amar 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: 1099014 - camphor 5.25 % / eucalyptus oil 1.6 % / menthol 3.15 % Topical Ointment
  • RxCUI: 1099014 - camphor 0.0525 MG/MG / Eucalyptus oil 0.016 MG/MG / menthol 0.0315 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".