Label: RADIATION PLUS- chondrus crispus, fucus vesiculosus, thyroidinum (suis), cadmium iodatum, cadmium sulphuratum, iodium, uranium nitricum, radium bromatum, strontium carbonicum, x-ray, arnica montana liquid

  • NDC Code(s): 43742-0491-1
  • Packager: Deseret Biologicals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated April 6, 2017

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS:

    Chondrus crispus 3X, Fucus vesiculosus 3X, Thyroidinum (Suis) 8X, Cadmium iodatum 12X, Cadmium sulphuratum 12X, Iodium 12X, Uranium nitricum 12X, Radium bromatum 12X, Strontium carbonicum 12X, X-Ray 30X, 60X, 200X, 30C, 60C, Arnica Montana 30C, 60C.

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  • HOMEOPATHIC INDICATIONS:

    For temporary relief from symptoms associated with radiation exposure, including weakness, fatigue, dehydration, diarrhea, and mental confusion.**

    **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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  • WARNINGS:

    Keep out of reach of children. In case of overdose, contact physician or Poison Control Center right away.

    If pregnant or breast-feeding, ask a health professional before use.

    Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.

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  • KEEP OUT OF REACH OF CHILDREN.

    KEEP OUT OF REACH OF CHILDREN. In case of overdose, contact physician or Poison Control Center right away.

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  • DIRECTIONS:

    1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

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  • HOMEOPATHIC INDICATIONS:

    For temporary relief from symptoms associated with radiation exposure, including weakness, fatigue, dehydration, diarrhea, and mental confusion.**

    **These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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  • INACTIVE INGREDIENTS:

    Demineralized water, 25% Ethanol.

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  • QUESTIONS:

    Dist. By: Deseret Biologicals, Inc.

    469 W. Parkland Drive

    Sandy, UT 84070

    www.desbio.com

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  • PACKAGE LABEL DISPLAY:

    DESBIO

    NDC 43742-0491-1

    HOMEOPATHIC

    RADIATION PLUS

    1 FL OZ (30 ml)

    Radiation Plus

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  • INGREDIENTS AND APPEARANCE
    RADIATION PLUS 
    chondrus crispus, fucus vesiculosus, thyroidinum (suis), cadmium iodatum, cadmium sulphuratum, iodium, uranium nitricum, radium bromatum, strontium carbonicum, x-ray, arnica montana liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0491
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHONDRUS CRISPUS (UNII: OQS23HUA1X) (CHONDRUS CRISPUS - UNII:OQS23HUA1X) CHONDRUS CRISPUS 3 [hp_X]  in 1 mL
    FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M) FUCUS VESICULOSUS 3 [hp_X]  in 1 mL
    SUS SCROFA THYROID (UNII: 6RV024OAUQ) (SUS SCROFA THYROID - UNII:6RV024OAUQ) SUS SCROFA THYROID 8 [hp_X]  in 1 mL
    CADMIUM IODIDE (UNII: 2F2UPU4KCW) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM IODIDE 12 [hp_X]  in 1 mL
    CADMIUM SULFIDE (UNII: 057EZR4Z7Q) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM SULFIDE 12 [hp_X]  in 1 mL
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 12 [hp_X]  in 1 mL
    URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE 12 [hp_X]  in 1 mL
    RADIUM BROMIDE (UNII: R74O7T8569) (RADIUM CATION - UNII:05456MVL7T) RADIUM BROMIDE 12 [hp_X]  in 1 mL
    STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (STRONTIUM CATION - UNII:37077S2C93) STRONTIUM CARBONATE 12 [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) 30 [hp_X]  in 1 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 30 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43742-0491-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 12/03/2015 08/25/2021
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 06/21/2014 08/25/2021
    Labeler - Deseret Biologicals, Inc. (940741853)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(43742-0491) , api manufacture(43742-0491) , label(43742-0491) , pack(43742-0491)
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