NDC 43742-1184 Ebv/cfs Plus

Carduus Marianus, Cistus Canadensis, Dulcamara, Galium Aparine, Magnesia Muriatica, Natrum Sulphuricum, Viscum Album, Muriaticum Acidum, Folliculinum, Aqua Marina, Ailanthus Glandulosa, Baryta Muriatica, Cadmium Metallicum, Ceanothus Americanus, Cocculus Indicus, Iridium Metallicum, Thuja Occidentalis, Cinchona Officinalis, Calcarea Carbonica, Crotalus Cascavella

NDC Product Code 43742-1184

NDC CODE: 43742-1184

Proprietary Name: Ebv/cfs Plus 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: Carduus Marianus, Cistus Canadensis, Dulcamara, Galium Aparine, Magnesia Muriatica, Natrum Sulphuricum, Viscum Album, Muriaticum Acidum, Folliculinum, Aqua Marina, Ailanthus Glandulosa, Baryta Muriatica, Cadmium Metallicum, Ceanothus Americanus, Cocculus Indicus, Iridium Metallicum, Thuja Occidentalis, Cinchona Officinalis, Calcarea Carbonica, Crotalus Cascavella 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 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1184-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Ebv/cfs Plus with NDC 43742-1184 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Ebv/cfs Plus is carduus marianus, cistus canadensis, dulcamara, galium aparine, magnesia muriatica, natrum sulphuricum, viscum album, muriaticum acidum, folliculinum, aqua marina, ailanthus glandulosa, baryta muriatica, cadmium metallicum, ceanothus americanus, cocculus indicus, iridium metallicum, thuja occidentalis, cinchona officinalis, calcarea carbonica, crotalus cascavella. 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.

Ebv/cfs Plus 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.

  • MILK THISTLE 6 [hp_X]/mL
  • HELIANTHEMUM CANADENSE 6 [hp_X]/mL
  • SOLANUM DULCAMARA TOP 6 [hp_X]/mL
  • GALIUM APARINE 6 [hp_X]/mL
  • MAGNESIUM CHLORIDE 6 [hp_X]/mL
  • SODIUM SULFATE 6 [hp_X]/mL
  • VISCUM ALBUM FRUITING TOP 6 [hp_X]/mL
  • HYDROCHLORIC ACID 6 [hp_X]/mL
  • ESTRONE 8 [hp_X]/mL
  • SODIUM CHLORIDE 10 [hp_X]/mL
  • AILANTHUS ALTISSIMA FLOWERING TWIG 12 [hp_X]/mL
  • BARIUM CHLORIDE DIHYDRATE 12 [hp_X]/mL
  • CADMIUM 12 [hp_X]/mL
  • CEANOTHUS AMERICANUS LEAF 12 [hp_X]/mL
  • ANAMIRTA COCCULUS SEED 12 [hp_X]/mL
  • IRIDIUM 12 [hp_X]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 12 [hp_X]/mL
  • CINCHONA OFFICINALIS BARK 12 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • CROTALUS DURISSUS TERRIFICUS VENOM 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 DRUG OTHER - 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: 03-15-2018 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.

Ebv/cfs Plus Product Label Images

Ebv/cfs Plus 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:

Carduus Marianus 6X, Cistus Canadensis 6X, Dulcamara 6X, Galium Aparine 6X, Magnesia Muriatica 6X, Natrum Sulphuricum 6X, Viscum Album 6X, Muriaticum Acidum 6X, 12X, 30X, Folliculinum 8X, 12X, 30X, Aqua Marina 10X, Ailanthus Glandulosa 12X, Baryta Muriatica 12X, Cadmium Metallicum 12X, Ceanothus Americanus 12X, Cocculus Indicus 12X, Iridium Metallicum 12X, Thuja Occidentalis 12X, Cinchona Officinalis 12X, 18X, 24X, 30X, Calcarea Carbonica 12X, 30X, Crotalus Cascavella 16X.

Homeopathic Indications:

For temporary relief of symptoms related to viral infections such as fever, fatigue, lack of appetite, rash, sore throat, swollen glands in neck, weakness of muscles, sore muscles, swelling of tonsils, chills, headaches.****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 viral infections such as fever, fatigue, lack of appetite, rash, sore throat, swollen glands in neck, weakness of muscles, sore muscles, swelling of tonsils, chills, headaches.****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.WARNING: Severe or persistent sore throat or sore throat accompanied by high fever, headache, nausea, and vomiting may be serious. Consult a physician promptly. Do not use more than two days or administer to children under 3 years of age unless directed by a physician.

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 43742-1184-1HOMEOPATHICEBV/CFSPLUS1 FL OZ (30 ml)

* Please review the disclaimer below.