NDC 43742-0984 Rheumagesic

Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Rhododendron Chrysanthum, Ruta Graveolens, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum

NDC Product Code 43742-0984

NDC CODE: 43742-0984

Proprietary Name: Rheumagesic 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: Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Rhododendron Chrysanthum, Ruta Graveolens, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum 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 43742-0984-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Rheumagesic with NDC 43742-0984 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Rheumagesic is arnica montana, apis mellifica, benzoicum acidum, cartilago suis, ledum palustre, pantothenic acid, rhododendron chrysanthum, ruta graveolens, causticum, formica rufa, sepia, alpha-lipoicum acidum, aurum metallicum, calcarea phosphorica, phytolacca decandra, radium bromatum, rhus venenata, thuja occidentalis, lac caninum. 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.

Rheumagesic 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.

  • ARNICA MONTANA 3 [hp_X]/mL
  • APIS MELLIFERA 6 [hp_X]/mL
  • BENZOIC ACID 6 [hp_X]/mL
  • SUS SCROFA CARTILAGE 6 [hp_X]/mL
  • RHODODENDRON TOMENTOSUM LEAFY TWIG 6 [hp_X]/mL
  • PANTOTHENIC ACID 6 [hp_X]/mL
  • RHODODENDRON AUREUM LEAF 6 [hp_X]/mL
  • RUTA GRAVEOLENS FLOWERING TOP 6 [hp_X]/mL
  • CAUSTICUM 10 [hp_X]/mL
  • FORMICA RUFA 10 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 10 [hp_X]/mL
  • THIOCTIC ACID 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 12 [hp_X]/mL
  • RADIUM BROMIDE 12 [hp_X]/mL
  • TOXICODENDRON VERNIX LEAFY TWIG 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
  • CANIS LUPUS FAMILIARIS MILK 16 [hp_X]/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: 02-21-2017 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: 03-06-2023 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.

Rheumagesic Product Label Images

Rheumagesic 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:

Arnica Montana 3X, Apis Mellifica 6X, Benzoicum Acidum 6X, Cartilago Suis 6X, Ledum Palustre 6X, Pantothenic Acid 6X, Rhododendron Chrysanthum 6X, Ruta Graveolens 6X, Causticum 10X, Formica Rufa 10X, Sepia 10X, alpha-Lipoicum Acidum 12X, Aurum Metallicum 12X, Calcarea Phosphorica 12X, Phytolacca Decandra 12X, Radium Bromatum 12X, Rhus Venenata 12X, Thuja Occidentalis 12X, Lac Caninum 16X.

Homeopathic Indications:

For temporary relief of symptoms related to arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. ****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 arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. ****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 physician or 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, contact physician or a 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 43742-0984-1HOMEOPATHICRHEUMAGESIC1 FL OZ (30 ml)

* Please review the disclaimer below.