Radiation

Manufacturer: The Wellness Center for Research and Education, Inc. | Apotheca Company
Effective date: 2025-06-04
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 20:37:17

Label at a glance#

ProductRadiation

Active ingredientCHELIDONIUM MAJUS, FUCUS VESICULOSUS, HYPERICUM PERFORATUM, SULFUR, CESIUM CHLORIDE, SUS SCROFA ADRENAL GLAND, SUS SCROFA THYROID, STRONTIUM CARBONATE, CADMIUM IODIDE, CADMIUM SULFATE, ALCOHOL, X-RAY EXPOSED (1000 RAD), RADIUM BROMIDE, URANYL NITRATE HEXAHYDRATE, LACTOSE, PLUTONIUM

Label structure9 sections

Dosage and administration

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

Contacts and useful links#

PhoneLabel contact1-866-962-6484

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

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:

OTC - PURPOSE SECTION

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:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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

INDICATIONS:

INDICATIONS & USAGE SECTION

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:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol

QUESTIONS:

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr. Theresa Dale's

NDC 50181-0043-1

Homeopathic

RADIATION

EMR, EMF, X-RAY, NUC

1 fl oz (30 ml)

Radiation

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ALCOHOL, X-RAY EXPOSED (1000 RAD)	ACTIVE INGREDIENT	6PRJ93602P	1
CADMIUM IODIDE	ACTIVE INGREDIENT	2F2UPU4KCW	1
CADMIUM SULFATE	ACTIVE INGREDIENT	947UNF3Z6O	1
CESIUM CHLORIDE	ACTIVE INGREDIENT	GNR9HML8BA	1
CHELIDONIUM MAJUS	ACTIVE INGREDIENT	7E889U5RNN	1
FUCUS VESICULOSUS	ACTIVE INGREDIENT	535G2ABX9M	1
HYPERICUM PERFORATUM	ACTIVE INGREDIENT	XK4IUX8MNB	1
LACTOSE	ACTIVE INGREDIENT	J2B2A4N98G	1
PLUTONIUM	ACTIVE INGREDIENT	53023GN24M	1
RADIUM BROMIDE	ACTIVE INGREDIENT	R74O7T8569	1
STRONTIUM CARBONATE	ACTIVE INGREDIENT	41YPU4MMCA	1
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	1
SUS SCROFA ADRENAL GLAND	ACTIVE INGREDIENT	398IYQ16YV	1
SUS SCROFA THYROID	ACTIVE INGREDIENT	6RV024OAUQ	1
URANYL NITRATE HEXAHYDRATE	ACTIVE INGREDIENT	3V057702FY	1
ALCOHOL, X-RAY EXPOSED (1000 RAD)	ACTIVE MOIETY	6PRJ93602P	1
ANHYDROUS LACTOSE	ACTIVE MOIETY	3SY5LH9PMK	1
CADMIUM CATION	ACTIVE MOIETY	T494FZ4G8G	1
CESIUM CATION	ACTIVE MOIETY	LCC4BG14DM	1
CHELIDONIUM MAJUS	ACTIVE MOIETY	7E889U5RNN	1
FUCUS VESICULOSUS	ACTIVE MOIETY	535G2ABX9M	1
HYPERICUM PERFORATUM	ACTIVE MOIETY	XK4IUX8MNB	1
PLUTONIUM	ACTIVE MOIETY	53023GN24M	1
RADIUM CATION	ACTIVE MOIETY	05456MVL7T	1
STRONTIUM CATION	ACTIVE MOIETY	37077S2C93	1
SULFUR	ACTIVE MOIETY	70FD1KFU70	1
SUS SCROFA ADRENAL GLAND	ACTIVE MOIETY	398IYQ16YV	1
SUS SCROFA THYROID	ACTIVE MOIETY	6RV024OAUQ	1
URANIUM CATION (6+)	ACTIVE MOIETY	5PI36AS4G7	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 25 matching rows.

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
CHELIDONIUM MAJUS
FUCUS VESICULOSUS
HYPERICUM PERFORATUM
SULFUR
CESIUM CHLORIDE
CESIUM CATION
SUS SCROFA ADRENAL GLAND
SUS SCROFA THYROID
STRONTIUM CARBONATE
STRONTIUM CATION
CADMIUM IODIDE
CADMIUM CATION
CADMIUM SULFATE
ALCOHOL, X-RAY EXPOSED (1000 RAD)
RADIUM BROMIDE
RADIUM CATION
URANYL NITRATE HEXAHYDRATE
URANIUM CATION (6+)
LACTOSE
ANHYDROUS LACTOSE
PLUTONIUM
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50181-0043	50181-0043-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CHELIDONIUM MAJUS	7E889U5RNN	ACTIB
FUCUS VESICULOSUS	535G2ABX9M	ACTIB
HYPERICUM PERFORATUM	XK4IUX8MNB	ACTIB
SULFUR	70FD1KFU70	ACTIB
CESIUM CHLORIDE	GNR9HML8BA	ACTIB
SUS SCROFA ADRENAL GLAND	398IYQ16YV	ACTIB
SUS SCROFA THYROID	6RV024OAUQ	ACTIB
STRONTIUM CARBONATE	41YPU4MMCA	ACTIB
CADMIUM IODIDE	2F2UPU4KCW	ACTIB
CADMIUM SULFATE	947UNF3Z6O	ACTIB
ALCOHOL, X-RAY EXPOSED (1000 RAD)	6PRJ93602P	ACTIB
RADIUM BROMIDE	R74O7T8569	ACTIB
URANYL NITRATE HEXAHYDRATE	3V057702FY	ACTIB
LACTOSE	J2B2A4N98G	ACTIB
PLUTONIUM	53023GN24M	ACTIB
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, FOAM / TOPICAL		4504 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TRANSDERMAL		7360 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SWAB / TOPICAL		2250 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / BUCCAL	679 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	PASTE / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TOPICAL		541 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / NASAL	70 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / SUBCUTANEOUS	6.1 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / INTRAVENOUS		4000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVENOUS	92 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	POWDER, FOR SOLUTION / TOPICAL	40 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVESICAL		7892 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY, METERED / SUBLINGUAL		29 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / RECTAL	0.35 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAMUSCULAR		1000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / RESPIRATORY (INHALATION)	0.08 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	JELLY / VAGINAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAVENOUS		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SHAMPOO / TOPICAL		714 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVASCULAR	100 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	35.75 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVENOUS		99 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAMUSCULAR		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / NASAL	20 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / RECTAL		898 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TRANSDERMAL		3675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAVENOUS		6405 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / RESPIRATORY (INHALATION)		26664 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, EMULSION / INTRAVENOUS		520 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / SUBCUTANEOUS		149 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TRANSDERMAL	49.37 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	MOUTHWASH / BUCCAL	200 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / DENTAL	12.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TOPICAL		9971 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAMUSCULAR		1491 mg	Exact identifier — unii candidate 59 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
b007b3fb-7b27-42a2-b7e4-1cf14137fc66			4d0115c9-edcb-4f0c-99e5-2ccce115b79a	2025-06-04	Warnings	Exact identifier spl id: b007b3fb-7b27-42a2-b7e4-1cf14137fc66 spl set id: 4d0115c9-edcb-4f0c-99e5-2ccce115b79a

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.