NDC 55146-004 4 Detox-virus

Astragalus Membranaceus, Baptisia Tinctoria, Echinacea (echinacea), Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Aranea Diadema, Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Lachesis Mutus, Phosphoricum Acidum, Silicea, Thuja Occidentalis, Vaccinium Myrtillus

NDC Product Code 55146-004

NDC Code: 55146-004

Proprietary Name: 4 Detox-virus 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: Astragalus Membranaceus, Baptisia Tinctoria, Echinacea (echinacea), Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Aranea Diadema, Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Lachesis Mutus, Phosphoricum Acidum, Silicea, Thuja Occidentalis, Vaccinium Myrtillus 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

  • 55146 - Biotics Research Corporation
    • 55146-004 - 4 Detox-virus

NDC 55146-004-01

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Product Information

4 Detox-virus with NDC 55146-004 is a a human over the counter drug product labeled by Biotics Research Corporation. The generic name of 4 Detox-virus is astragalus membranaceus, baptisia tinctoria, echinacea (echinacea), phytolacca decandra, hydrastis canadensis, apis mellifica, aranea diadema, belladonna, eupatorium perfoliatum, gelsemium sempervirens, lachesis mutus, phosphoricum acidum, silicea, thuja occidentalis, vaccinium myrtillus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Biotics Research Corporation

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.

4 Detox-virus 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.

  • ASTRAGALUS PROPINQUUS ROOT 3 [hp_X]/mL
  • BAPTISIA TINCTORIA 3 [hp_X]/mL
  • ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
  • GOLDENSEAL 5 [hp_X]/mL
  • APIS MELLIFERA 30 [hp_C]/mL
  • ARANEUS DIADEMATUS 30 [hp_C]/mL
  • ARSENIC TRIOXIDE 30 [hp_C]/mL
  • ATROPA BELLADONNA 30 [hp_C]/mL
  • EUPATORIUM PERFOLIATUM FLOWERING TOP 30 [hp_C]/mL
  • GELSEMIUM SEMPERVIRENS ROOT 30 [hp_C]/mL
  • LACHESIS MUTA VENOM 30 [hp_C]/mL
  • PHOSPHORIC ACID 30 [hp_C]/mL
  • RANCID BEEF 30 [hp_C]/mL
  • SILICON DIOXIDE 30 [hp_C]/mL
  • THUJA OCCIDENTALIS LEAFY TWIG 30 [hp_C]/mL
  • BILBERRY 30 [hp_C]/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)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

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: Biotics Research Corporation
Labeler Code: 55146
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: 06-11-2019 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.

4 Detox-virus Product Label Images

4 Detox-virus 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:

Astragalus Membranaceus 3X, 30C, Baptisia Tinctoria 3X, 30C, Echinacea 3X, 30C, Phytolacca Decandra 4X, 30C, Hydrastis Canadensis 5X, 30C, Apis Mellifica 30C, Aranea Diadema 30C, Arsenicum Album 30C, Belladonna 30C, Eupatorium Perfoliatum 30C, Gelsemium Sempervirens 30C, Lachesis Mutus 30C, Phosphoricum Acidum 30C, Pyrogenium 30C, Silicea 30C, Thuja Occidentalis 30C, Vaccinium Myrtillus 30C.

Indications:

For temporary relief of skin irritation, dry cough, eczema or fever. Remedy #4 supports detoxification of residual toxins left from a viral infection.

For temporary relief of skin irritation, dry cough, eczema or fever. Remedy #4 supports detoxification of residual toxins left from a viral infection.

Warnings:

If symptoms persist or worsen, seek the advice of a healthcare professional.Caution: Not recommended for pregnant or lactating women.KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.Tamper Seal: Sealed for your protection with a clear, full body seal. 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, get medical help or contact a Poison Control Center right away.

Directions:

One (1) teaspoon twice daily or as otherwise directed by a healthcare professional. Consult a physician for use in children under 6 years of age.

Inactive Ingredients:

Citric acid, Demineralized water, Ethanol and Sodium benzoate.

Questions:

Distributed byBiotics Research CorporationRosenberg, TX 77471 • (281) 344-0909

Package Label Display:

Biotics Research Corporation's21st CENTURYHOMEOPATHICSNDC #55146-004-01HOMEOPATHIC REMEDY#4Detox-VirusWater BasedFormula(1.91% Ethanol)4 fl. oz. (120ml)

* Please review the disclaimer below.

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