NDC 50181-0055 Biotox Hep

Cochlearia Armoracia, Chelidonium Majus, Arsenicum Album, Hepar Suis, Spleen (suis), Thymus (suis), Hepatitis C Nosode, Hepatitis A Nosode, Hepatitis B Nosode

NDC Product Code 50181-0055

NDC Code: 50181-0055

Proprietary Name: Biotox Hep 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: Cochlearia Armoracia, Chelidonium Majus, Arsenicum Album, Hepar Suis, Spleen (suis), Thymus (suis), Hepatitis C Nosode, Hepatitis A Nosode, Hepatitis B Nosode 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

  • 50181 - The Wellness Center For Research And Education, Inc.
    • 50181-0055 - Biotox Hep

NDC 50181-0055-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Biotox Hep with NDC 50181-0055 is a a human over the counter drug product labeled by The Wellness Center For Research And Education, Inc.. The generic name of Biotox Hep is cochlearia armoracia, chelidonium majus, arsenicum album, hepar suis, spleen (suis), thymus (suis), hepatitis c nosode, hepatitis a nosode, hepatitis b nosode. The product's dosage form is liquid and is administered via oral form.

Labeler Name: The Wellness Center For Research And Education, 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.

Biotox Hep 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.

  • HORSERADISH 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • ARSENIC TRIOXIDE 6 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA SPLEEN 8 [hp_X]/mL
  • SUS SCROFA THYMUS 8 [hp_X]/mL
  • HEPATITIS C VIRUS 17 [hp_X]/mL
  • HEPATITIS A VIRUS 17 [hp_X]/mL
  • HEPATITIS B VIRUS 32 [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: The Wellness Center For Research And Education, Inc.
Labeler Code: 50181
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: 10-15-2015 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: 12-31-2019 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.

Biotox Hep Product Label Images

Biotox Hep 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:

Cochlearia Armoracia 3X, Chelidonium Majus 3X, 6X, 8X, Arsenicum Album 6X, 8X, 12X, 30C, Hepar Suis 8X, 12X 30C, Spleen (Suis) 8X, 30C, Thymus (Suis) 8X, 1LM, Hepatitis C Nosode 17X, 30C, 60C, 1M, Hepatitis A Nosode 17X, 30C, 3LM, Hepatitis B Nosode 32X, 30C, 3LM.

Indications:

Fatigue, fever, cough, flu-like symptoms, virus, pain, swelling, and stiffness of limbs.

Fatigue, fever, cough, flu-like symptoms, virus, pain, swelling, and stiffness of limbs.

Warnings:

If pregnant or breast-feeding, ask a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store in a cool, dry place.

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:

5 drops 2 or 3 times per day, on an empty stomach, 5 days per week or until symptoms abate. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

MFD FOR:The Wellness Center forResearch and Education, Inc.1237 S. Victoria Ave. Suite 169Oxnard CA 930351-866-962-6484

Package Label Display:

Dr. Theresa Dale'sNDC 50181-0055-1HomeopathicBioToxHep1 fl oz (30 ml)

* Please review the disclaimer below.

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