FDA.reportPublic FDA data

Radiation

Manufacturer
BioActive Nutritional | Apotheca Company
Effective date
2024-09-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:27:55

Label at a glance#

ProductRadiation
Active ingredientCAPSICUM, CETRARIA ISLANDICA WHOLE, FUCUS VESICULOSUS, SUS SCROFA ADRENAL GLAND, THYROID, CADMIUM IODIDE, HYDRANGEA ARBORESCENS ROOT, PHOSPHORIC ACID, PHOSPHORUS, PULSATILLA PRATENSIS WHOLE, STRONTIUM CARBONATE, URANYL NITRATE HEXAHYDRATE, ALCOHOL, X-RAY EXPOSED (1000 RAD)
Label structure9 sections

Dosage and administration

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION


Capsicum Annuum 3X, Cetraria Islandica 3X, Fucus Vesiculosus 3X, Glandula Suprarenalis Suis 8X, Thyroidinum (Suis) 8X, Cadmium Iodatum 12X, Hydrangea Arborescens 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Pulsatilla (Pratensis) 12X, Strontium Carbonicum 12X, Uranium Nitricum 30X, X-Ray 30X, 60X, 200X, 30C, 60C.

INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of cough with expectoration, skin cracked with eruptions and weakness and trembling of arms and hands with numbness.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care 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 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

10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

For temporary relief of cough with expectoration, skin cracked with eruptions and weakness and trembling of arms and hands with numbness.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Distributed by:

BioActive Nutritional, Inc.

1803 N. Wickham Rd.

Melbourne, FL 32935

bioactivenutritional.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOActive Nutritional

RADIATION

HOMEOPATHIC

1 FL OZ (30 ml)

RadiationRadiation

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43857-0540-12024-09-11C16284748780-1d6a99b39-d3ac-a426-e053-dadaa90af4c2Drug Facts:
43857-0540-12022-01-28C16284748780-1d6a99b39-d3ac-a426-e053-dadaa90af4c2Drug Facts:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43857-0540-1Radiation30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43857-0540RADIATION (CAPSICUM ANNUUM, CETRARIA ISLANDICA, FUCUS VESICULOSUS, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (SUIS), CADMIUM IODATUM, HYDRANGEA ARBORESCENS, PHOSPHORICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STRONTIUM CARBONICUM, URANIUM NITRICUM, X-RAY) LIQUID [BIOACTIVE NUTRITIONAL]2Current NDC, Legacy NDC, 1 package rows20240913_1c49738c-6750-47de-a623-96f53eab7bad.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43857-054043857-0540-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPSICUM00UK7646FGACTIB
CETRARIA ISLANDICA WHOLEBJ7YPN79A1ACTIB
FUCUS VESICULOSUS535G2ABX9MACTIB
SUS SCROFA ADRENAL GLAND398IYQ16YVACTIB
THYROID6RV024OAUQACTIB
CADMIUM IODIDE2F2UPU4KCWACTIB
HYDRANGEA ARBORESCENS ROOTSFK828Q2DEACTIB
PHOSPHORIC ACIDE4GA8884NNACTIB
PHOSPHORUS27YLU75U4WACTIB
PULSATILLA PRATENSIS WHOLE8E272251DIACTIB
STRONTIUM CARBONATE41YPU4MMCAACTIB
URANYL NITRATE HEXAHYDRATE3V057702FYACTIB
ALCOHOL, X-RAY EXPOSED (1000 RAD)6PRJ93602PACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
RadiationCAPSICUM ANNUUM, CETRARIA ISLANDICA, FUCUS VESICULOSUS, GLANDULA SUPRARENALIS SUIS, THYROIDINUM (SUIS), CADMIUM IODATUM, HYDRANGEA ARBORESCENS, PHOSPHORICUM ACIDUM, PHOSPHORUS, PULSATILLA (PRATENSIS), STRONTIUM CARBONICUM, URANIUM NITRICUM, X-RAYBioActive Nutritional1c49738c-6750-47de-a623-96f53eab7bad2024-09-11WarningsExact identifier
ndc (package): 43857-0540-1
ndc (product): 43857-0540
ndc11 (package): 43857054001
spl id: b7adf3e4-9cc6-4db4-9e8e-83a068f9cdf3
spl set id: 1c49738c-6750-47de-a623-96f53eab7bad

Reported adverse events (FAERS/openFDA)#

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