NDC 43742-0452 Breathe Rxs

Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Natrum Muriaticum, Rhus Tox, Sulphur, Adenosinum Cyclophosphoricum, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Lung (suis), Mucosa Nasalis Suis, Sarcolacticum Acidum, Acetylcholine Chloride, Coumarinum, Malvin, Dysentery Bacillus, Morgan Bacillus (pure)

NDC Product Code 43742-0452

NDC CODE: 43742-0452

Proprietary Name: Breathe Rxs What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Aconitum Napellus, Argentum Nitricum, Arsenicum Album, Natrum Muriaticum, Rhus Tox, Sulphur, Adenosinum Cyclophosphoricum, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Lung (suis), Mucosa Nasalis Suis, Sarcolacticum Acidum, Acetylcholine Chloride, Coumarinum, Malvin, Dysentery Bacillus, Morgan Bacillus (pure) What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available
  • Arsenic trioxide is used to treat a type of leukemia (acute promyelocytic leukemia-APL).
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0452-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Breathe Rxs with NDC 43742-0452 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Breathe Rxs is aconitum napellus, argentum nitricum, arsenicum album, natrum muriaticum, rhus tox, sulphur, adenosinum cyclophosphoricum, coenzyme a, funiculus umbilicalis suis, glandula suprarenalis suis, lung (suis), mucosa nasalis suis, sarcolacticum acidum, acetylcholine chloride, coumarinum, malvin, dysentery bacillus, morgan bacillus (pure). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Breathe Rxs Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACONITUM NAPELLUS 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • ARSENIC TRIOXIDE 6 [hp_X]/mL
  • SODIUM CHLORIDE 6 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • ADENOSINE CYCLIC PHOSPHATE 10 [hp_X]/mL
  • COENZYME A 10 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 10 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 10 [hp_X]/mL
  • SUS SCROFA LUNG 10 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA 10 [hp_X]/mL
  • LACTIC ACID, L- 10 [hp_X]/mL
  • ACETYLCHOLINE CHLORIDE 6 [hp_C]/mL
  • COUMARIN 6 [hp_C]/mL
  • MALVIN 15 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 03-11-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 02-03-2021 What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

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Breathe Rxs Product Label Images

Breathe Rxs Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Aconitum napellus 6X, 10X, 30X, Argentum nitricum 6X, 10X, 30X, Arsenicum album 6X, 10X, 30X, Natrum muriaticum 6X, 10X, 30X, Rhus tox 6X, 10X, 30X, Sulphur 6X, 10X, 30X, Adenosinum cyclophosphoricum 10X, Coenzyme A 10X, Funiculus umbilicalis suis 10X, Glandula suprarenalis suis 10X, Lung (suis) 10X, Mucosa nasalis suis 10X, Sarcolacticum acidum 10X, Acetylcholine chloride 6C, 30C, 200C, Coumarinum 6C, 30C, 200C, Malvin 15C, 30C, 200C, Dysentery bacillus 30C, Morgan bacillus (Pure) 30C.

Indications:

For temporary relief of symptoms related to the respiratory system.

For temporary relief of symptoms related to the respiratory system.

Warnings:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: sealed for your protection.  Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops under the tongue, three times per day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 25% Ethanol.

Questions:

Dist. by DesBio, Inc.     www.desbio.com469 Parkland Drive, Sandy UT 84070

Package Label Display:

DESBIONDC 43742-0452-1BREATHE RXSHOMEOPATHIC SUPPORT1 FL OZ (30 ML)

* Please review the disclaimer below.