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  4. NDC Product Code: 59970-048 Vaporizing Chest Rub

NDC 59970-048 Vaporizing Chest Rub

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59970-048?
  4. Vaporizing Chest Rub Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59970-048
Proprietary Name:
Vaporizing Chest Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Narvarro Discount Pharmarcies,llc
Labeler Code:
59970
Product Label ID:
d54be1a1-10e3-43ec-b54e-aa7bd7e8be20
Start Marketing Date: [9]
08-15-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 59970-048?

The NDC code 59970-048 is assigned by the FDA to the product Vaporizing Chest Rub which is product labeled by Narvarro Discount Pharmarcies,llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59970-048-04 113 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 Rub?

See important warnings under "When using this product"adults and children 2 years and over:Apply a thick layer on chest and throat or rub on sore aching muscles.Cover with a warm, dry cloth if desiredKeep clothing loose about throat/chest to help vapors reach the nose/mouthrepeat up to 3 times per 24 hours or as directed by doctorchildren under 2 years: do not use

Which are Vaporizing Chest Rub UNII Codes?

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

Which are 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:

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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".