NDC 43742-1094 Nausia

Zingiber Officinale, Cyclamen Europaeum, Ipecacuanha, Iris Versicolor, Lac Defloratum, Lacticum Acidum, Tabacum, Petroleum, Euphorbia Corollata, Arsenicum Album, Bryonia (alba), Cadmium Sulphuratum, Cocculus Indicus, Colchicum Autumnale, Conium Maculatum, Ferrum Metallicum, Nux Vomica, Pulsatilla (pratensis), Sepia, Theridion

NDC Product Code 43742-1094

NDC Code: 43742-1094

Proprietary Name: Nausia 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: Zingiber Officinale, Cyclamen Europaeum, Ipecacuanha, Iris Versicolor, Lac Defloratum, Lacticum Acidum, Tabacum, Petroleum, Euphorbia Corollata, Arsenicum Album, Bryonia (alba), Cadmium Sulphuratum, Cocculus Indicus, Colchicum Autumnale, Conium Maculatum, Ferrum Metallicum, Nux Vomica, Pulsatilla (pratensis), Sepia, 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.
    • 43742-1094 - Nausia

NDC 43742-1094-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Nausia with NDC 43742-1094 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Nausia is zingiber officinale, cyclamen europaeum, ipecacuanha, iris versicolor, lac defloratum, lacticum acidum, tabacum, petroleum, euphorbia corollata, arsenicum album, bryonia (alba), cadmium sulphuratum, cocculus indicus, colchicum autumnale, conium maculatum, ferrum metallicum, nux vomica, pulsatilla (pratensis), sepia, 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.

Nausia 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.

  • GINGER 3 [hp_X]/mL
  • CYCLAMEN PURPURASCENS TUBER 6 [hp_X]/mL
  • IPECAC 6 [hp_X]/mL
  • IRIS VERSICOLOR ROOT 6 [hp_X]/mL
  • SKIM MILK 6 [hp_X]/mL
  • LACTIC ACID, DL- 6 [hp_X]/mL
  • TOBACCO LEAF 6 [hp_X]/mL
  • KEROSENE 8 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • BRYONIA ALBA ROOT 12 [hp_X]/mL
  • CADMIUM SULFIDE 12 [hp_X]/mL
  • ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 12 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • ANEMONE PRATENSIS 12 [hp_X]/mL
  • SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
  • THERIDION CURASSAVICUM 12 [hp_X]/mL
  • EUPHORBIA COROLLATA ROOT 24 [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: 11-17-2017 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: 11-21-2022 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.

Nausia Product Label Images

Nausia 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:

Zingiber Officinale 3X, Cyclamen Europaeum 6X, Ipecacuanha 6X, Iris Versicolor 6X, Lac Defloratum 6X, Lacticum Acidum 6X, Tabacum 6X, Petroleum 8X, Arsenicum Album 12X, Bryonia (Alba) 12X, Cadmium Sulphuratum 12X, Cocculus Indicus 12X, Colchicum Autumnale 12X, Conium Maculatum 12X, Ferrum Metallicum 12X, Nux Vomica 12X, Pulsatilla (Pratensis) 12X, Sepia 12X, Theridion 12X, Euphorbia Corollata 24X.

Homeopathic Indications:

For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, and headache.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of the symptoms of nausea and vomiting associated with pain, pregnancy, vertigo, and headache.****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 Poison Control Center right away.If pregnant or breast-feeding, seek advice of 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 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 43742-1094-1HOMEOPATHICNAUSIA1 FL OZ (30 ml)

* Please review the disclaimer below.

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