NDC 55146-010 10 Parasite Detox

Carduus Marianus, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur

NDC Product Code 55146-010

NDC Code: 55146-010

Proprietary Name: 10 Parasite Detox 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, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur 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
    • 55146-010 - 10 Parasite Detox

NDC 55146-010-01

Package Description: 120 mL in 1 BOTTLE, PLASTIC

NDC Product Information

10 Parasite Detox with NDC 55146-010 is a a human over the counter drug product labeled by Biotics Research Corporation. The generic name of 10 Parasite Detox is carduus marianus, chelidonium majus, cina, sabadilla, teucrium marum, terebinthina, thyroidinum (suis), spigelia anthelmia, apis mellifica, baryta carbonica, calcarea carbonica, ferrum muriaticum, natrum muriaticum, silicea, sulphur. 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.

10 Parasite Detox 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 3 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • ARTEMISIA CINA PRE-FLOWERING TOP 3 [hp_X]/mL
  • SCHOENOCAULON OFFICINALE SEED 3 [hp_X]/mL
  • TEUCRIUM MARUM 3 [hp_X]/mL
  • TURPENTINE OIL 5 [hp_X]/mL
  • SUS SCROFA THYROID 6 [hp_X]/mL
  • SPIGELIA ANTHELMIA 6 [hp_X]/mL
  • APIS MELLIFERA 30 [hp_C]/mL
  • BARIUM CARBONATE 30 [hp_C]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 30 [hp_C]/mL
  • FERRIC CHLORIDE HEXAHYDRATE 30 [hp_C]/mL
  • SODIUM CHLORIDE 30 [hp_C]/mL
  • SILICON DIOXIDE 30 [hp_C]/mL
  • SULFUR 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.

10 Parasite Detox Product Label Images

10 Parasite Detox 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 3X, 30C, Chelidonium Majus 3X, 30C, Cina 3X, 30C, Sabadilla 3X, 30C, Teucrium Marum 3X, 30C, Terebinthina 5X, Thyroidinum (Suis) 6X, Spigelia Anthelmia 6X, 30C, Apis Mellifica 30C, Baryta Carbonica 30C, Calcarea Carbonica 30C, Ferrum Muriaticum 30C, Natrum Muriaticum 30C, Silicea 30C, Sulphur 30C.

Indications:

For temporary relief of fever, joint pain, cough, stiffness and gastric upset. Remedy #10 supports detoxification of toxins that remain following a parasitic infection.

For temporary relief of fever, joint pain, cough, stiffness and gastric upset. Remedy #10 supports detoxification of toxins that remain following a parasitic infection.

Warnings:

If symptoms persist or worsen, seek the advice of a healthcare professional.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Caution: Not recommended for pregnant or lactating women.Tamper Seal: Sealed for your protection with a clear, full body seal. Do not use if seal is missing or broken.

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 directed by a healthcare professional. Consult a physician for use in children under 6 years of age.

Inactive Ingredients:

Citric Acid, Demineralized Water, Ethanol, Sodium Benzoate

Questions:

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

Package Label Display:

Biotics Research Corporation's21st CENTURYHOMEOPATHICSNDC #55146-010-01HOMEOPATHIC REMEDY#10Chronic StressWater BasedFormula(1.1% Ethanol)4 fl. oz. (120ml)

* Please review the disclaimer below.

Previous Code
55146-009
Next Code
55147-001