NDC 43742-0944 Oratox

Fucus Vesiculosus, Lymph Node (suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis), Calcarea Muriatica, Iodium, Natrum Fluoratum, Natrum Muriaticum, Selenium Metallicum, Vanadium Metallicum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum

NDC Product Code 43742-0944

NDC CODE: 43742-0944

Proprietary Name: Oratox 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: Fucus Vesiculosus, Lymph Node (suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis), Calcarea Muriatica, Iodium, Natrum Fluoratum, Natrum Muriaticum, Selenium Metallicum, Vanadium Metallicum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum Metallicum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum 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
  • This medication is used to prevent cavities. It makes teeth stronger and more resistant to decay caused by acid and bacteria. Talk to your dentist or doctor about the benefits and risks of this product. This medication is not recommended for use in infants less than 6 months of age. This medication is not recommended for use in areas where the fluoride content in the water supply is greater than 0.6 parts per million. See Notes section for more information.
  • This product is used to treat dryness inside the nose (nasal passages). It helps add moisture inside the nose to dissolve and soften thick or crusty mucus. In babies and young children with stuffy noses who cannot blow their noses, using this product helps to make the mucus easier to remove with a nasal bulb syringe. This helps relieve stuffiness and makes breathing easier. This product contains a purified gentle salt solution (also called saline or sodium chloride solution). It does not contain any medication.
  • Drug uses not available
  • Drug uses not available
  • This medication is used as an antiperspirant to treat feet that sweat or smell excessively. It is also used as a drying agent during wart treatment.
  • This medication is used to relieve nerve pain after shingles (infection with the herpes zoster virus). This type of pain is called post-herpetic neuralgia. Lidocaine helps to reduce sharp/burning/aching pain as well as discomfort caused by skin areas that are overly sensitive to touch. Lidocaine belongs to a class of drugs known as local anesthetics. It works by causing a temporary loss of feeling in the area where you apply the patch.
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0944-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Oratox with NDC 43742-0944 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Oratox is fucus vesiculosus, lymph node (suis), medulla ossis suis, thymus (suis), thyroidinum (suis), calcarea muriatica, iodium, natrum fluoratum, natrum muriaticum, selenium metallicum, vanadium metallicum, argentum metallicum, aurum metallicum, cuprum metallicum, eugenol, formalinum, lidocaine, mercurius solubilis, molybdenum metallicum, niccolum metallicum, palladium metallicum, stannum metallicum, titanium metallicum, zincum metallicum. 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.

Oratox 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.

  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA BONE MARROW 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • CALCIUM CHLORIDE 12 [hp_X]/mL
  • IODINE 12 [hp_X]/mL
  • SODIUM FLUORIDE 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 1/mL
  • SELENIUM 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • EUGENOL 12 [hp_X]/mL
  • FORMALDEHYDE 12 [hp_X]/mL
  • LIDOCAINE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • TITANIUM 12 [hp_X]/mL
  • ZINC 12 [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: 12-27-2016 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Oratox Product Label Images

Oratox 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:

Fucus Vesiculosus 3X, Lymph Node (Suis) 8X, Medulla Ossis Suis 8X, Thymus (Suis) 8X, Thyroidinum (Suis) 8X, Calcarea Muriatica 12X, Iodium 12X, Natrum Fluoratum 12X, Natrum Muriaticum 12X, Selenium Metallicum 12X, Vanadium Metallicum 12X, Argentum Metallicum 12X, 30X, 60X, 200X, Aurum Metallicum 12X, 30X, 60X, 200X, Cuprum Metallicum 12X, 30X, 60X, 200X, Eugenol 12X, 30X, 60X, 200X, Formalinum 12X, 30X, 60X, 200X, Lidocaine 12X, 30X, 60X, 200X, Mercurius Solubilis 12X, 30X, 60X, 200X, Molybdenum Metallicum 12X, 30X, 60X, 200X, Niccolum Metallicum 12X, 30X, 60X, 200X, Palladium Metallicum 12X, 30X, 60X, 200X, Stannum Metallicum 12X, 30X, 60X, 200X, Titanium Metallicum 12X, 30X, 60X, 200X, Zincum Metallicum 12X, 30X, 60X, 200X.

Homeopathic Indications:

For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, inflammation, and joint pain.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms related to heavy metal toxicity caused by toxic dental materials in the mouth. These include muscle cramps, inflammation, and joint pain.****These statements are based upon traditional 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 43742-0944-1HOMEOPATHICORATOX1 FL OZ (30 ml)

* Please review the disclaimer below.