NDC 43742-0434 Rheumatoid Arthritis Nosode

Atp (adenosine Triphosphate Disodium), Malic Acid, Natrum Oxalaceticum, Riboflavinum, Apiolum, Cinnamic Acid, Dhea (dehydroepiandrosterone), Streptococcus Viridans

NDC Product Code 43742-0434

NDC Code: 43742-0434

Proprietary Name: Rheumatoid Arthritis Nosode 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: Atp (adenosine Triphosphate Disodium), Malic Acid, Natrum Oxalaceticum, Riboflavinum, Apiolum, Cinnamic Acid, Dhea (dehydroepiandrosterone), Streptococcus Viridans 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.
    • 43742-0434 - Rheumatoid Arthritis Nosode

NDC 43742-0434-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Rheumatoid Arthritis Nosode with NDC 43742-0434 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Rheumatoid Arthritis Nosode is atp (adenosine triphosphate disodium), malic acid, natrum oxalaceticum, riboflavinum, apiolum, cinnamic acid, dhea (dehydroepiandrosterone), streptococcus viridans. 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.

Rheumatoid Arthritis Nosode 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.

  • ADENOSINE TRIPHOSPHATE DISODIUM 6 [hp_X]/mL
  • MALIC ACID 6 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
  • OROTIC ACID MONOHYDRATE 6 [hp_X]/mL
  • RIBOFLAVIN 6 [hp_X]/mL
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • CINNAMIC ACID 6 [hp_X]/mL
  • PRASTERONE 6 [hp_X]/mL
  • STREPTOCOCCUS VIRIDANS GROUP 12 [hp_X]/mL
  • BORRELIA BURGDORFERI 15 [hp_X]/mL
  • BRUCELLA ABORTUS 15 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 15 [hp_X]/mL
  • CAMPYLOBACTER JEJUNI 15 [hp_X]/mL
  • CHLAMYDIA TRACHOMATIS 15 [hp_X]/mL
  • KLEBSIELLA PNEUMONIAE 15 [hp_X]/mL
  • MYCOPLASMA PNEUMONIAE 15 [hp_X]/mL
  • YERSINIA ENTEROCOLITICA 17 [hp_X]/mL
  • STREPTOCOCCUS PNEUMONIAE 17 [hp_X]/mL
  • STREPTOCOCCUS AGALACTIAE 9 [hp_C]/mL
  • ENTEROCOCCUS FAECALIS 13 [hp_C]/mL
  • STREPTOCOCCUS MUTANS 13 [hp_C]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 14 [hp_C]/mL
  • SHIGELLA DYSENTERIAE 15 [hp_C]/mL
  • SHIGELLA SONNEI 15 [hp_C]/mL
  • STREPTOCOCCUS DYSGALACTIAE 15 [hp_C]/mL
  • STREPTOCOCCUS PYOGENES 15 [hp_C]/mL
  • STREPTOCOCCUS UBERIS 15 [hp_C]/mL
  • PROTEUS MORGANII 30 [hp_C]/mL
  • STREPTOCOCCUS EQUINUS 32 [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: 07-11-2014 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

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’.

* Please review the disclaimer below.

Rheumatoid Arthritis Nosode Product Label Images

Rheumatoid Arthritis Nosode 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:

ATP (Adenosine Triphosphate Disodium) 6X, Malic Acid 6X, Natrum Oxalaceticum 6X, Oroticum Acidum 6X, Riboflavinum 6X, Apiloum 6X, 8X, 10X, 30X, 200X, Cinnamic Acid 6X, 8X, 10X, 30X, 200X, DHEA (Dehydroepiandrosterone) 6X, 8X, 10X, 30X, 200X, Streptococcus viridians 12X, 33X,  Borrelia Burgdorferi Nosode 15X, 30X, 100X, 200X, Brucella Abortus 15X, 30X,100X, 200X, Calcarea Carbonica 15X, 30X, 100X, 200X, Campylobacter Jejuni 15X, 30X, 100X, 200X, Chlamydia Trachomatis 15X, 30X, 100X, 200X, Klebseiella Pneumoniae 15X, 30X, 100X, 200X, Mycoplasma Pneumoniae 15X, 30X, 100X, 200X, Yersinia Enterocolitica 17X, 30X, 100X, 200X, Streptococcus Pneumoniae 17X, 13C, Streptococcus agalactiae 9C, Enterococcus Faecalis 13C, Streptococcus Mutans 13C, Salmonella Enteritidis 14C, 30C, 100C, 200C, Dysentery Bacillus 15C, Shigella Sonnei 15C, Streptococcus Dysgalactiae 15C, Streptococcus Pyogenes 15C, Streptococcus Uberis 15C, Morgan Bach (Proteus Morgani) 30C, Streptococcus Bovis 32C.

Indications:

For the temporary relief of Rheumatoid Arthritis Symptoms such as joint pain and inflammation.

For the temporary relief of Rheumatoid Arthritis Symptoms such as joint pain and inflammation.

Warnings:

Keep out of reach of children. In case of overdose, contact 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 Parkland DriveSandy, UT 84070  www.desbio.com

Package Label Display

DESBIONDC 43742-0434-1HOMEOPATHICRHEUMATOID ARTHRITIS  NOSODE

* Please review the disclaimer below.

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