NDC 43742-0590 Intestinal Distress

Echinacea (angustifolia), Colchicum Autumnale, Aloe, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album, Clostridium Difficile, Chininum Sulphuricum, Cholera Nosode, Campylobacter Jejuni, Colibacillinum Cum Natrum Muriaticum, Helicobacter Pylori, Shigella, Yersinia Enterocolitica, Botulinum Nosode, Salmonella Typhi Nosode, Brugia Malayi

NDC Product Code 43742-0590

NDC Code: 43742-0590

Proprietary Name: Intestinal Distress 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: Echinacea (angustifolia), Colchicum Autumnale, Aloe, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album, Clostridium Difficile, Chininum Sulphuricum, Cholera Nosode, Campylobacter Jejuni, Colibacillinum Cum Natrum Muriaticum, Helicobacter Pylori, Shigella, Yersinia Enterocolitica, Botulinum Nosode, Salmonella Typhi Nosode, Brugia Malayi 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0590-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Intestinal Distress with NDC 43742-0590 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Intestinal Distress is echinacea (angustifolia), colchicum autumnale, aloe, colocynthis, mercurius corrosivus, nux vomica, arsenicum album, clostridium difficile, chininum sulphuricum, cholera nosode, campylobacter jejuni, colibacillinum cum natrum muriaticum, helicobacter pylori, shigella, yersinia enterocolitica, botulinum nosode, salmonella typhi nosode, brugia malayi. 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.

Intestinal Distress 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.

  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 4 [hp_X]/mL
  • ALOE 6 [hp_X]/mL
  • CITRULLUS COLOCYNTHIS FRUIT PULP 6 [hp_X]/mL
  • MERCURIC CHLORIDE 6 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 6 [hp_X]/mL
  • ARSENIC TRIOXIDE 6 [hp_X]/mL
  • CLOSTRIDIUM DIFFICILE 8 [hp_X]/mL
  • QUININE SULFATE 12 [hp_X]/mL
  • VIBRIO CHOLERAE 12 [hp_X]/mL
  • CAMPYLOBACTER JEJUNI 30 [hp_X]/mL
  • ESCHERICHIA COLI 30 [hp_X]/mL
  • HELICOBACTER PYLORI 30 [hp_X]/mL
  • SHIGELLA DYSENTERIAE 30 [hp_X]/mL
  • YERSINIA ENTEROCOLITICA 30 [hp_X]/mL
  • BOTULINUM TOXIN TYPE A 30 [hp_X]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI 33 [hp_X]/mL
  • BRUGIA MALAYI 39 [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.

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: 07-10-2015 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: 12-29-2022 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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Intestinal Distress Product Label Images

Intestinal Distress 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:

Echinacea (Angustifolia) 3X, Colchicum Autumnale 4X, Aloe 6X, Colocynthis 6X, Mercurius Corrosivus 6X, Nux Vomica 6X, Arsenicum Album 6X, 12X, 30X, Clostridium Difficile 8X, 30X, Chininum Sulphuricum 12X, Cholera Nosode 12X, 30X, Campylobacter Jejuni 30X, Colibacillinum Cum Natrum Muriaticum 30X, Helicobacter Pylori 30X, Shigella 30X, Yersinia Enterocolitica 30X, Botulinum Nosode 30X, 60X, Salmonella Typhi Nosode 33X, Brugia Malayi 39C, 60C, 200C.

Indications:

For temporary relief of symptoms related to gastroenteritis including diarrhea, stomach cramps, nausea, vomiting, fluid and electrolyte depletion, flatulence and bloating.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to gastroenteritis including diarrhea, stomach cramps, nausea, vomiting, fluid and electrolyte depletion, flatulence and bloating.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.If pregnant or breast-feeding, seek advice of 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, contact a physician or Poison Control Center right away.

Directions:

1-10 drops under the tongue, 3 times a 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: Deseret Biologicals, Inc.469 W. Parkland DriveSandy, UT 84070     www.desbio.com

Package Label Display:

DESBIONDC 43742-0590-1HOMEOPATHICINTESTINALDISTRESS1 FL OZ (30 ml)

* Please review the disclaimer below.