NDC 43742-1646 Tinitx

Allium Cepa, Argentum Nitricum, Chenopodium Anthelminticum, Dulcamara, Ginkgo Biloba, Chininum Sulphuricum, Cartilago Suis, Mucosa Nasalis Suis, Asarum Canadense, Onosmodium Virginianum, Natrum Salicylicum, Carbo Vegetabilis, Carboneum Sulphuratum, Cyclamen Europaeum, Gossypium Herbaceum, Graphites, Kreosotum, Phosphorus, Plumbum Metallicum, Theridion, Zincum Metallicum

NDC Product Code 43742-1646

NDC CODE: 43742-1646

Proprietary Name: Tinitx 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: Allium Cepa, Argentum Nitricum, Chenopodium Anthelminticum, Dulcamara, Ginkgo Biloba, Chininum Sulphuricum, Cartilago Suis, Mucosa Nasalis Suis, Asarum Canadense, Onosmodium Virginianum, Natrum Salicylicum, Carbo Vegetabilis, Carboneum Sulphuratum, Cyclamen Europaeum, Gossypium Herbaceum, Graphites, Kreosotum, Phosphorus, Plumbum Metallicum, Theridion, 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 alone or with other medication to treat malaria caused by mosquito bites in countries where malaria is common. Malaria parasites can enter the body through these mosquito bites, and then live in body tissues such as red blood cells or the liver. This medication is used to kill the malaria parasites living inside red blood cells. In some cases, you may need to take a different medication (such as primaquine) to kill the malaria parasites living in other body tissues. Both drugs may be needed for a complete cure and to prevent the return of infection (relapse). Quinine belongs to a class of drugs known as antimalarials. It is not used for the prevention of malaria. The United States Centers for Disease Control provide updated guidelines and travel recommendations for the prevention and treatment of malaria in different parts of the world. Discuss the most recent information with your doctor before traveling to areas where malaria occurs.
  • Drug uses not available
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1646-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Tinitx with NDC 43742-1646 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Tinitx is allium cepa, argentum nitricum, chenopodium anthelminticum, dulcamara, ginkgo biloba, chininum sulphuricum, cartilago suis, mucosa nasalis suis, asarum canadense, onosmodium virginianum, natrum salicylicum, carbo vegetabilis, carboneum sulphuratum, cyclamen europaeum, gossypium herbaceum, graphites, kreosotum, phosphorus, plumbum metallicum, theridion, 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.

Tinitx 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.

  • ONION 6 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • DYSPHANIA AMBROSIOIDES WHOLE 6 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 6 [hp_X]/mL
  • GINKGO 6 [hp_X]/mL
  • QUININE SULFATE 6 [hp_X]/mL
  • SUS SCROFA CARTILAGE 8 [hp_X]/mL
  • SUS SCROFA NASAL MUCOSA 8 [hp_X]/mL
  • ASARUM CANADENSE ROOT 9 [hp_X]/mL
  • ONOSMODIUM VIRGINIANUM 10 [hp_X]/mL
  • SODIUM SALICYLATE 10 [hp_X]/mL
  • ACTIVATED CHARCOAL 12 [hp_X]/mL
  • CARBON DISULFIDE 12 [hp_X]/mL
  • CYCLAMEN PURPURASCENS TUBER 12 [hp_X]/mL
  • GOSSYPIUM HERBACEUM ROOT BARK 12 [hp_X]/mL
  • GRAPHITE 12 [hp_X]/mL
  • WOOD CREOSOTE 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • LEAD 12 [hp_X]/mL
  • THERIDION CURASSAVICUM 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: 05-29-2020 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: 12-31-2021 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.

Tinitx Product Label Images

Tinitx 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:

Allium Cepa 6X, Argentum Nitricum 6X, Chenopodium Anthelminticum 6X, Dulcamara 6X, Ginkgo Biloba 6X, Chininum Sulphuricum 6X, 12X, 30X, 200X, Cartilago Suis 8X, 12X, 30X, 200X, Mucosa Nasalis Suis 8X, 12X, 30X, 200X, Asarum Canadense 9X, Onosmodium Virginianum 10X, Natrum Salicylicum 10X, 12X, 30X, 200X, Carbo Vegetabilis 12X, Carboneum Sulphuratum 12X, Cyclamen Europaeum 12X, Gossypium Herbaceum 12X, Graphites 12X, Kreosotum 12X, Phosphorus 12X, Plumbum Metallicum 12X, Theridion 12X, Zincum Metallicum 12X.

Homeopathic Indications:

For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .****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 a physician or 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 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 W. Parkland DriveSandy, UT 84070 www.desbio.com

Package Label Display:

DESBIONDC 43742-1646-1HOMEOPATHICTinitX1 FL OZ (30 ml)

* Please review the disclaimer below.