NDC 43742-0668 Chronagesic

Dulcamara, Arnica Montana, Rhus Tox, Sanguinaria Canadensis, Cartilago Suis, Coenzyme A, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Placenta Totalis Suis, Sulphur, Chondroitin Sulphate Sodium (bovine), Methylsulfonylmethane (msm), Apiolum, Cinnamic Acid, Menadione, Piperine, Alpha-lipoicum Acidum, Silicea, Symphytum Officinale, Human Growth Hormone, Gaertner Bacillus, Sycotic Co Bacillus

NDC Product Code 43742-0668

NDC Code: 43742-0668

Proprietary Name: Chronagesic 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: Dulcamara, Arnica Montana, Rhus Tox, Sanguinaria Canadensis, Cartilago Suis, Coenzyme A, Funiculus Umbilicalis Suis, Nadidum, Natrum Oxalaceticum, Placenta Totalis Suis, Sulphur, Chondroitin Sulphate Sodium (bovine), Methylsulfonylmethane (msm), Apiolum, Cinnamic Acid, Menadione, Piperine, Alpha-lipoicum Acidum, Silicea, Symphytum Officinale, Human Growth Hormone, Gaertner Bacillus, Sycotic Co Bacillus 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 43742-0668-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Chronagesic with NDC 43742-0668 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Chronagesic is dulcamara, arnica montana, rhus tox, sanguinaria canadensis, cartilago suis, coenzyme a, funiculus umbilicalis suis, nadidum, natrum oxalaceticum, placenta totalis suis, sulphur, chondroitin sulphate sodium (bovine), methylsulfonylmethane (msm), apiolum, cinnamic acid, menadione, piperine, alpha-lipoicum acidum, silicea, symphytum officinale, human growth hormone, gaertner bacillus, sycotic co bacillus. 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.

Chronagesic 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.

  • SOLANUM DULCAMARA TOP 2 [hp_X]/mL
  • ARNICA MONTANA 3 [hp_X]/mL
  • TOXICODENDRON PUBESCENS LEAF 3 [hp_X]/mL
  • SANGUINARIA CANADENSIS ROOT 3 [hp_X]/mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/mL
  • COENZYME A 6 [hp_X]/mL
  • SUS SCROFA UMBILICAL CORD 6 [hp_X]/mL
  • NADIDE 6 [hp_X]/mL
  • SODIUM DIETHYL OXALACETATE 6 [hp_X]/mL
  • SUS SCROFA PLACENTA 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • CHONDROITIN SULFATE SODIUM (BOVINE) 6 [hp_X]/mL
  • DIMETHYL SULFONE 6 [hp_X]/mL
  • APIOLE (PARSLEY) 6 [hp_X]/mL
  • CINNAMIC ACID 6 [hp_X]/mL
  • MENADIONE 6 [hp_X]/mL
  • PIPERINE 6 [hp_X]/mL
  • .ALPHA.-LIPOIC ACID 8 [hp_X]/mL
  • SILICON DIOXIDE 8 [hp_X]/mL
  • COMFREY ROOT 8 [hp_X]/mL
  • SOMATROPIN 30 [hp_X]/mL
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • ENTEROCOCCUS FAECALIS 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.

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: 12-03-2015 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: 03-31-2021 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’.

* Please review the disclaimer below.

Chronagesic Product Label Images

Chronagesic 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:

Dulcamara 2X, Arnica Montana 3X, Rhus Tox 3X, Sanguinaria Canadensis 3X, Cartilago Suis 6X, Coenzyme A 6X, Funiculus Umbilicalis Suis 6X, Nadidum 6X, Natrum Oxalaceticum 6X, Placenta Totalis Suis 6X, Sulphur 6X, Chondroitin Sulphate Sodium (Bovine) 6X, 12X, 30X, 200X, Methylsulfonylmethane (MSM) 6X, 12X, 30X, 200X, Apiolum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Cinnamic Acid 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Menadione 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Piperine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Alpha-Lipoicum Acidum 8X, Silicea 8X, Symphytum Officinale 8X, Human Growth Hormone 30X, Gaertner Bacillus 30C, Sycotic Co Bacillus 30C.

Homeopathic Indications:

For temporary relief of mild to moderate arthritic pain and joint stiffness.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of mild to moderate arthritic pain and joint stiffness.****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, 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, 3 to 6 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: Deseret Biologicals, Inc. • www.desbio.com469 W. Parkland Drive • Sandy, UT 84070

Package Label Display:

DESBIONDC43742-0668-1CHRONAGESICHomeopathic Management of Mild to Moderate Pain1 FL OZ (30 ml)

* Please review the disclaimer below.