NDC 43742-0829 Mucous Membrane Core Formula

Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectal Mucosa (suis), Stomach (suis), Sulphur

NDC Product Code 43742-0829

NDC CODE: 43742-0829

Proprietary Name: Mucous Membrane Core Formula 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: Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectal Mucosa (suis), Stomach (suis), Sulphur 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

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0829-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Mucous Membrane Core Formula with NDC 43742-0829 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Mucous Membrane Core Formula is ceanothus americanus, veratrum album, anacardium orientale, argentum nitricum, condurango, hydrastis canadensis, momordica balsamina, oxalis acetosella, pulsatilla (vulgaris), bile duct (suis), colon (suis), duodenum (suis), esophagus (suis), eye (suis), gallbladder (suis), ileum (suis), intestine (suis), ipecacuanha, jejunum (suis), kali bichromicum, lung (suis), mucosa nasalis suis, natrum oxalaceticum, oral mucosa (suis), pancreas suis, phosphorus, rectal mucosa (suis), stomach (suis), sulphur. 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.

Mucous Membrane Core Formula 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.

  • CEANOTHUS AMERICANUS LEAF 4 [hp_X]/mL
  • VERATRUM ALBUM ROOT 4 [hp_X]/mL
  • SEMECARPUS ANACARDIUM JUICE 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • MARSDENIA CONDURANGO BARK 6 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • MOMORDICA BALSAMINA IMMATURE FRUIT 6 [hp_X]/mL
  • OXALIS ACETOSELLA LEAF 6 [hp_X]/mL
  • PULSATILLA VULGARIS 6 [hp_X]/mL
  • SUS SCROFA BILE DUCT 8 [hp_X]/mL
  • SUS SCROFA COLON 8 [hp_X]/mL
  • SUS SCROFA DUODENUM 8 [hp_X]/mL
  • SUS SCROFA ESOPHAGUS 8 [hp_X]/mL
  • SUS SCROFA EYE 8 [hp_X]/mL
  • SUS SCROFA GALLBLADDER 8 [hp_X]/mL
  • SUS SCROFA ILEUM 8 [hp_X]/mL
  • SUS SCROFA LARGE INTESTINE 8 [hp_X]/mL
  • PORK INTESTINE 8 [hp_X]/mL
  • IPECAC 8 [hp_X]/mL
  • SUS SCROFA JEJUNUM 8 [hp_X]/mL
  • POTASSIUM DICHROMATE 8 [hp_X]/mL
  • SUS SCROFA LUNG 8 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA 8 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
  • SUS SCROFA ORAL MUCOSA 8 [hp_X]/mL
  • SUS SCROFA PANCREAS 8 [hp_X]/mL
  • PHOSPHORUS 8 [hp_X]/mL
  • SUS SCROFA RECTAL MUCOSA 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL
  • YEAST MANNAN 8 [hp_X]/mL
  • ATROPA BELLADONNA 10 [hp_X]/mL
  • WOOD CREOSOTE 10 [hp_X]/mL
  • LACHESIS MUTA VENOM 10 [hp_X]/mL
  • MANDRAGORA OFFICINARUM ROOT 10 [hp_X]/mL
  • SUS SCROFA URINARY BLADDER 6 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 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: 08-17-2016 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: 03-07-2022 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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Mucous Membrane Core Formula Product Label Images

Mucous Membrane Core Formula 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:

Ceanothus Americanus 4X, Veratrum Album 4X, Anacardium Orientale 6X, Argentum Nitricum 6X, Condurango 6X, Hydrastis Canadensis 6X, Momordica Balsamina 6X, Oxalis Acetosella 6X, Pulsatilla (Vulgaris) 6X, Bile Duct (Suis) 8X, Colon (Suis) 8X, Duodenum (Suis) 8X, Esophagus (Suis) 8X, Eye (Suis) 8X, Gallbladder (Suis) 8X, Ileum (Suis) 8X, Intestine (Suis) 8X, Ipecacuanha 8X, Jejunum (Suis) 8X, Kali Bichromicum 8X, Lung (Suis) 8X, Mucosa Nasalis Suis 8X, Natrum Oxalaceticum 8X, Oral Mucosa (Suis) 8X, Pancreas Suis 8X, Phosphorus 8X, Rectal Mucosa (Suis) 8X, Stomach (Suis) 8X, Sulphur 8X, Mannan 8X, 30X, 200X, Belladonna 10, Kreosotum 10X, Lachesis Mutus 10X, Mandragora Officinarum 10X, Urinary Bladder (Suis) 6C, Dysentery Bacillus 30C, 200C.

Homeopathic Indications:

Temporary relief of symptoms related to congestion of the many mucous membranes of the body including GI disturbance, chronic allergies, and anxieties.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Temporary relief of symptoms related to congestion of the many mucous membranes of the body including GI disturbance, chronic allergies, and anxieties.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store at room temperature.Keep out of direct sunlight.

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:

Adults 3-10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

DISTRIBUTED BY:Deseret Biologicals, Inc., Sandy, UT 84070800.827.9529      www.desbio.com

Package Label Display:

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0829-1HOMEOPATHICMUCOUS MEMBRANECore FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.