NDC 50181-0043 Radiation

Chelidonium Majus, Fucus Vesiculosus, Hypericum Perforatum, Sulphur, Cesium Chloride, Glandula Suprarenalis Suis, Thyroidinum (suis), Strontium Carbonicum, Cadmium Iodatum, Cadmium Sulphuricum, X-ray, Radium Bromatum, Uranium Nitricum, Electricitas, Plutonium Nitricum

NDC Product Code 50181-0043

NDC Code: 50181-0043

Proprietary Name: Radiation 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: Chelidonium Majus, Fucus Vesiculosus, Hypericum Perforatum, Sulphur, Cesium Chloride, Glandula Suprarenalis Suis, Thyroidinum (suis), Strontium Carbonicum, Cadmium Iodatum, Cadmium Sulphuricum, X-ray, Radium Bromatum, Uranium Nitricum, Electricitas, Plutonium Nitricum 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.


Code Structure
  • 50181 - The Wellness Center For Research And Education, Inc.
    • 50181-0043 - Radiation

NDC 50181-0043-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Radiation with NDC 50181-0043 is a a human over the counter drug product labeled by The Wellness Center For Research And Education, Inc.. The generic name of Radiation is chelidonium majus, fucus vesiculosus, hypericum perforatum, sulphur, cesium chloride, glandula suprarenalis suis, thyroidinum (suis), strontium carbonicum, cadmium iodatum, cadmium sulphuricum, x-ray, radium bromatum, uranium nitricum, electricitas, plutonium nitricum. 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.


Radiation 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.

  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • FUCUS VESICULOSUS 3 [hp_X]/mL
  • HYPERICUM PERFORATUM 6 [hp_X]/mL
  • SULFUR 6 [hp_X]/mL
  • CESIUM CHLORIDE 6 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • STRONTIUM CARBONATE 8 [hp_X]/mL
  • CADMIUM IODIDE 8 [hp_X]/mL
  • CADMIUM SULFATE 8 [hp_X]/mL
  • ALCOHOL, X-RAY EXPOSED (1000 RAD) 8 [hp_X]/mL
  • RADIUM BROMIDE 15 [hp_X]/mL
  • URANYL NITRATE HEXAHYDRATE 8 [hp_C]/mL
  • LACTOSE 30 [hp_C]/mL
  • PLUTONIUM 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)

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.

* Please review the disclaimer below.

Radiation Product Label Images

Radiation 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:

Chelidonium Majus 3X, Fucus Vesiculosus 3X, Hypericum Perforatum 6X, Sulphur 6X, Cesium Chloride 6X, 30C, 200C, Glandula Suprarenalis Suis 8X, Thyroidinum (Suis) 8X, Strontium Carbonicum 8X, 12X, 30X, Cadmium Iodatum 8X, 15X, 30X, Cadmium Sulphuricum 8X, 15X, 30X, X-Ray 8X, 60X, 200X, 30C, Radium Bromatum 15X, Uranium Nitricum 8C, 30C, 60C, Electricitas 30C, Plutonium Nitricum 30C.

Indications:

For temporary relief of fatigue, weakness, burning skin eruptions, itching, trembling of limbs with numbness, cough with phlegm, fever, sticking pains in head and face.  Vomiting, warty growths.

For temporary relief of fatigue, weakness, burning skin eruptions, itching, trembling of limbs with numbness, cough with phlegm, fever, sticking pains in head and face. Vomiting, warty growths.

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 orally, three times daily.  Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

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

Package Label Display

Dr. Theresa Dale'sNDC 50181-0043-1HomeopathicRADIATIONEMR, EMF, X-RAY, NUC1 fl oz (30 ml)

* Please review the disclaimer below.

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