NDC 43742-1340 Vertigone

Natrum Salicylicum, Cerebellum (suis), Bryonia (alba), Petroleum, Tabacum, Ambra Grisea, Cyclamen Europaeum, Argentum Nitricum, Asarum Canadense, Calcarea Sulphurica, Carboneum Sulphuratum, Chininum Sulphuricum, Cocculus Indicus, Conium Maculatum, Digitalis Purpurea, Gelsemium Sempervirens, Phosphorus, Piper Methysticum, Silicea, Theridion

NDC Product Code 43742-1340

NDC Code: 43742-1340

Proprietary Name: Vertigone 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: Natrum Salicylicum, Cerebellum (suis), Bryonia (alba), Petroleum, Tabacum, Ambra Grisea, Cyclamen Europaeum, Argentum Nitricum, Asarum Canadense, Calcarea Sulphurica, Carboneum Sulphuratum, Chininum Sulphuricum, Cocculus Indicus, Conium Maculatum, Digitalis Purpurea, Gelsemium Sempervirens, Phosphorus, Piper Methysticum, Silicea, Theridion 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.
    • 43742-1340 - Vertigone

NDC 43742-1340-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Vertigone with NDC 43742-1340 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Vertigone is natrum salicylicum, cerebellum (suis), bryonia (alba), petroleum, tabacum, ambra grisea, cyclamen europaeum, argentum nitricum, asarum canadense, calcarea sulphurica, carboneum sulphuratum, chininum sulphuricum, cocculus indicus, conium maculatum, digitalis purpurea, gelsemium sempervirens, phosphorus, piper methysticum, silicea, theridion. 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.

Vertigone 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.

  • SODIUM SALICYLATE 3 [hp_X]/mL
  • SUS SCROFA CEREBELLUM 6 [hp_X]/mL
  • BRYONIA ALBA ROOT 8 [hp_X]/mL
  • KEROSENE 8 [hp_X]/mL
  • TOBACCO LEAF 8 [hp_X]/mL
  • AMBERGRIS 9 [hp_X]/mL
  • CYCLAMEN PURPURASCENS TUBER 9 [hp_X]/mL
  • SILVER NITRATE 12 [hp_X]/mL
  • ASARUM CANADENSE ROOT 12 [hp_X]/mL
  • CALCIUM SULFATE ANHYDROUS 12 [hp_X]/mL
  • CARBON DISULFIDE 12 [hp_X]/mL
  • QUININE SULFATE 12 [hp_X]/mL
  • ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
  • DIGITALIS 12 [hp_X]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • MACROPIPER METHYSTICUM ROOT 12 [hp_X]/mL
  • SILICON DIOXIDE 12 [hp_X]/mL
  • THERIDION CURASSAVICUM 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.

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: 05-28-2019 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.

Vertigone Product Label Images

Vertigone 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:

Natrum Salicylicum 3X, Cerebellum (Suis) 6X, 12X, 30X, 200X, Bryonia (Alba) 8X, Petroleum 8X, Tabacum 8X, Ambra Grisea 9X, Cyclamen Europaeum 9X, Argentum Nitricum 12X, Asarum Canadense 12X, Calcarea Sulphurica 12X, Carboneum Sulphuratum 12X, Chininum Sulphuricum 12X, Cocculus Indicus 12X, Conium Maculatum 12X, Digitalis Purpurea 12X, Gelsemium Sempervirens 12X, Phosphorus 12X, Piper Methysticum 12X, Silicea 12X, Theridion 12X.

Homeopathic Indications:

For temporary relief of symptoms of vertigo such as faintness, vomiting, motion sickness, spinning or swaying sensation and weakness.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For temporary relief of symptoms of vertigo such as faintness, vomiting, motion sickness, spinning or swaying sensation and weakness.****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 43742-1340-1HOMEOPATHICVERTIGONE1 FL OZ (30 ml)

* Please review the disclaimer below.

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