Search by Drug Name or NDC

NDC 50181-0043-01 Radiation 8; 8; 8; 6; 3; 3; 6; 30; 30; 15; 8; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL Details

Radiation 8; 8; 8; 6; 3; 3; 6; 30; 30; 15; 8; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL

Radiation is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Wellness Center for Research and Education, Inc.. The primary component is ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM IODIDE; CADMIUM SULFATE; CESIUM CHLORIDE; CHELIDONIUM MAJUS; FUCUS VESICULOSUS; HYPERICUM PERFORATUM; LACTOSE; PLUTONIUM; RADIUM BROMIDE; STRONTIUM CARBONATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYROID;.

Product Information

NDC	50181-0043
Product ID	50181-0043_05b13696-c2ab-4590-b884-dd2341617548
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Radiation
Proprietary Name Suffix	n/a
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, Pluto
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	ORAL
Active Ingredient Strength	8; 8; 8; 6; 3; 3; 6; 30; 30; 15; 8; 6; 8; 8; 8
Active Ingredient Units	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL
Substance Name	ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM IODIDE; CADMIUM SULFATE; CESIUM CHLORIDE; CHELIDONIUM MAJUS; FUCUS VESICULOSUS; HYPERICUM PERFORATUM; LACTOSE; PLUTONIUM; RADIUM BROMIDE; STRONTIUM CARBONATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYROID;
Labeler Name	The Wellness Center for Research and Education, Inc.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	UNAPPROVED HOMEOPATHIC
Application Number	n/a
Listing Certified Through	2024-12-31

Package

Package Images

NDC 50181-0043-01 (50181004301)

Pricing Information	N/A
NDC Package Code	50181-0043-1
Billing NDC	50181004301
Package	30 mL in 1 BOTTLE, DROPPER (50181-0043-1)
Marketing Start Date	2014-05-13
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 4d0115c9-edcb-4f0c-99e5-2ccce115b79a Details

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.

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.

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.

INACTIVE INGREDIENTS:

Demineralized Water, 25% Ethanol

QUESTIONS:

MFD FOR:

The Wellness Center for Research and Education, Inc.

1237 S. Victoria Ave. Suite 169

Oxnard, CA 93035

1-866-962-6484

PACKAGE LABEL DISPLAY

Dr. Theresa Dale's

NDC 50181-0043-1

Homeopathic

RADIATION

EMR, EMF, X-RAY, NUC

1 fl oz (30 ml)

INGREDIENTS AND APPEARANCE

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 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:50181-0043
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CHELIDONIUM MAJUS (UNII: 7E889U5RNN) (CHELIDONIUM MAJUS - UNII:7E889U5RNN)	CHELIDONIUM MAJUS	3 [hp_X] in 1 mL
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M)	FUCUS VESICULOSUS	3 [hp_X] in 1 mL
HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (HYPERICUM PERFORATUM - UNII:XK4IUX8MNB)	HYPERICUM PERFORATUM	6 [hp_X] in 1 mL
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	6 [hp_X] in 1 mL
CESIUM CHLORIDE (UNII: GNR9HML8BA) (CESIUM CATION - UNII:LCC4BG14DM)	CESIUM CHLORIDE	6 [hp_X] in 1 mL
SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV)	SUS SCROFA ADRENAL GLAND	8 [hp_X] in 1 mL
SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ)	SUS SCROFA THYROID	8 [hp_X] in 1 mL
STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (STRONTIUM CATION - UNII:37077S2C93)	STRONTIUM CARBONATE	8 [hp_X] in 1 mL
CADMIUM IODIDE (UNII: 2F2UPU4KCW) (CADMIUM CATION - UNII:T494FZ4G8G)	CADMIUM IODIDE	8 [hp_X] in 1 mL
CADMIUM SULFATE (UNII: 947UNF3Z6O) (CADMIUM CATION - UNII:T494FZ4G8G)	CADMIUM SULFATE	8 [hp_X] in 1 mL
ALCOHOL, X-RAY EXPOSED (1000 RAD) (UNII: 6PRJ93602P) (ALCOHOL, X-RAY EXPOSED (1000 RAD) - UNII:6PRJ93602P)	ALCOHOL, X-RAY EXPOSED (1000 RAD)	8 [hp_X] in 1 mL
RADIUM BROMIDE (UNII: R74O7T8569) (RADIUM CATION - UNII:05456MVL7T)	RADIUM BROMIDE	15 [hp_X] in 1 mL
URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7)	URANYL NITRATE HEXAHYDRATE	8 [hp_C] in 1 mL
LACTOSE (UNII: J2B2A4N98G) (ANHYDROUS LACTOSE - UNII:3SY5LH9PMK)	LACTOSE	30 [hp_C] in 1 mL
PLUTONIUM (UNII: 53023GN24M) (PLUTONIUM - UNII:53023GN24M)	PLUTONIUM	30 [hp_C] in 1 mL

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:50181-0043-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/13/2014

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		05/13/2014

Labeler - The Wellness Center for Research and Education, Inc. (832363993)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(50181-0043) , api manufacture(50181-0043) , label(50181-0043) , pack(50181-0043)

Revised: 10/2017

Document Id: 05b13696-c2ab-4590-b884-dd2341617548

Set id: 4d0115c9-edcb-4f0c-99e5-2ccce115b79a

Version: 2

Effective Time: 20171020

Search by Drug Name or NDC

NDC 50181-0043-01 Radiation 8; 8; 8; 6; 3; 3; 6; 30; 30; 15; 8; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL Details

Radiation 8; 8; 8; 6; 3; 3; 6; 30; 30; 15; 8; 6; 8; 8; 8 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL

Product Information

Package

Package Images

NDC 50181-0043-01 (50181004301)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL 4d0115c9-edcb-4f0c-99e5-2ccce115b79a Details

ACTIVE INGREDIENTS:

INDICATIONS:

WARNINGS:

KEEP OUT OF REACH OF CHILDREN:

DIRECTIONS:

INDICATIONS:

INACTIVE INGREDIENTS:

QUESTIONS:

PACKAGE LABEL DISPLAY

INGREDIENTS AND APPEARANCE

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