NDC 57955-1803 Bronchialcare Soins Des Bronches

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:
57955-1803
Proprietary Name:
Bronchialcare Soins Des Bronches
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
King Bio Inc.
Labeler Code:
57955
Start Marketing Date: [9]
08-06-2014
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 57955-1803-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 57955-1803?

The NDC code 57955-1803 is assigned by the FDA to the product Bronchialcare Soins Des Bronches which is product labeled by King Bio Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57955-1803-2 59 ml in 1 bottle, spray . 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 Bronchialcare Soins Des Bronches?

Indications: A homeopathic remedy for the temporary relief of minor bronchial symptoms such as:shortness of breathtighness in chestwheezingbronchial irritationcoughminor breathing difficultiesIndications: Un reméde homéopathique pour le soulagement temporaire des symptômes bronchiques légers tels que:respiration courteserrement à la poitrinerespiration sifflanteirritation bronchiquetouxdifficultés mineures à respirer

Which are Bronchialcare Soins Des Bronches UNII Codes?

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

Which are Bronchialcare Soins Des Bronches 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:

* 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".