NDC 70359-4107 Breathiezzz

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:
70359-4107
Proprietary Name:
Breathiezzz
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fortunique B.v.
Labeler Code:
70359
Start Marketing Date: [9]
01-21-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70359-4107-1

Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON / 10 g in 1 TUBE, WITH APPLICATOR

Product Details

What is NDC 70359-4107?

The NDC code 70359-4107 is assigned by the FDA to the product Breathiezzz which is product labeled by Fortunique B.v.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70359-4107-1 1 tube, with applicator in 1 carton / 10 g in 1 tube, with applicator. 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 Breathiezzz?

See important warnings under " When using this product"Adults and children 2 years and over: roll layer on chest & throat or roll on sore aching muscles. Cover with a warm, dry cloth if desired. Keep clothing loose around throat /chest to help vapors reach the nose/mouth. Repeat up to three times per 24 hours or as directed by doctor. Children under 2 years: do not use

Which are Breathiezzz UNII Codes?

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

  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

Which are Breathiezzz 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".