Label: EMF- argentum nitricum, arnica montana, baptisia tinctoria, cinchona officinalis, galium aparine, hepar suis, natrum carbonicum, panax ginseng, phosphoricum acidum, phosphorus, rhododendron chrysanthum, strontium carbonicum, sulphur iodatum, thuja occidentalis, x-ray spray

  • NDC Code(s): 50845-0248-1
  • Packager: Liddell Laboratories, 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 9, 2019

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

  • ACTIVE INGREDIENTS:

    (in each spray): 6.67% of Argentum nitricum 30C, Arnica montana 3X, Baptisia tinctoria 3X, Cinchona officinalis 6X, Galium aparine 3X, Hepar suis 6X, Natrum carbonicum 200C, Panax ginseng 1X, Phosphorus 12X, Phosphoricum acidum 3X, Rhododendron Chrysanthum 30C, Strontium Carbonicum 12X, Sulphur iodatum 200C, Thuja occidentalis 200C, X-Ray 200C.

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  • USES:

    May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as:

    • recurring fatigue
    • nausea
    • disturbed sleep
    • frequent headaches
    • mental confusion**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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  • WARNINGS:

    Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

    Stop use and ask a doctor if symptoms persist, worsen or if new symptoms occur.

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

    If pregnant or breast feeding, ask a doctor before using product.

    Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.

    Store at room temperature.

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  • KEEP OUT OF REACH OF CHILDREN:

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

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  • DIRECTIONS:

    Adults and children over 12: Spray twice under the tongue three times per day for one month. For the next three months use same dosage one week per month.

    Children 12 and under: Consult a doctor prior to use.

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  • INDICATIONS:

    May temporarily aid in detoxifying the body and temporarily relieve symptoms of electromagnetic field (EMF) radiation exposure, such as:

    • recurring fatigue
    • nausea
    • disturbed sleep
    • frequent headaches
    • mental confusion**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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  • INACTIVE INGREDIENTS:

    Organic alcohol 20% v/v, Purified water.

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  • QUESTIONS:

    DIST. BY

    LIDDELL LABORATORIES

    201 APPLE BLVD.

    WOODBINE, IA 51579

    WWW.LIDDELL.NET

    1-800-460-7733

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  • PACKAGE LABEL DISPLAY:

    ORAL SPRAYS

    LIDDELL

    LABORATORIES


    EST. 1994

    DETOX

    48 EMF

    Electromagnetic

    Radiation

    May relieve symptoms of EMF
    radiation: fatigue, headache,
    disturbed sleep, confusion.


    HOMEOPATHIC

    DOCTOR FORMULATED

    Readily absorbed. Safe.

    No known side effects. Easy to use.

    1.0 FL OZ (30 ml)

    EMF

    EMF

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  • INGREDIENTS AND APPEARANCE
    EMF 
    argentum nitricum, arnica montana, baptisia tinctoria, cinchona officinalis, galium aparine, hepar suis, natrum carbonicum, panax ginseng, phosphoricum acidum, phosphorus, rhododendron chrysanthum, strontium carbonicum, sulphur iodatum, thuja occidentalis, x-ray spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50845-0248
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SILVER NITRATE (UNII: 95IT3W8JZE) (SILVER CATION - UNII:57N7B0K90A) SILVER NITRATE 30 [hp_C]  in 1 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 3 [hp_X]  in 1 mL
    BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 3 [hp_X]  in 1 mL
    CINCHONA OFFICINALIS BARK (UNII: S003A158SB) (CINCHONA OFFICINALIS BARK - UNII:S003A158SB) CINCHONA OFFICINALIS BARK 6 [hp_X]  in 1 mL
    GALIUM APARINE (UNII: Z4B6561488) (GALIUM APARINE - UNII:Z4B6561488) GALIUM APARINE 3 [hp_X]  in 1 mL
    PORK LIVER (UNII: 6EC706HI7F) (PORK LIVER - UNII:6EC706HI7F) PORK LIVER 6 [hp_X]  in 1 mL
    SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) SODIUM CARBONATE 200 [hp_C]  in 1 mL
    ASIAN GINSENG (UNII: CUQ3A77YXI) (ASIAN GINSENG - UNII:CUQ3A77YXI) ASIAN GINSENG 1 [hp_X]  in 1 mL
    PHOSPHORIC ACID (UNII: E4GA8884NN) (PHOSPHORIC ACID - UNII:E4GA8884NN) PHOSPHORIC ACID 3 [hp_X]  in 1 mL
    PHOSPHORUS (UNII: 27YLU75U4W) (PHOSPHORUS - UNII:27YLU75U4W) PHOSPHORUS 12 [hp_X]  in 1 mL
    RHODODENDRON AUREUM LEAF (UNII: IV92NQJ73U) (RHODODENDRON AUREUM LEAF - UNII:IV92NQJ73U) RHODODENDRON AUREUM LEAF 30 [hp_C]  in 1 mL
    STRONTIUM CARBONATE (UNII: 41YPU4MMCA) (STRONTIUM CATION - UNII:37077S2C93) STRONTIUM CARBONATE 12 [hp_X]  in 1 mL
    SULFUR IODIDE (UNII: L6L8KA2AA0) (SULFUR IODIDE - UNII:L6L8KA2AA0) SULFUR IODIDE 200 [hp_C]  in 1 mL
    THUJA OCCIDENTALIS LEAFY TWIG (UNII: 1NT28V9397) (THUJA OCCIDENTALIS LEAFY TWIG - UNII:1NT28V9397) THUJA OCCIDENTALIS LEAFY TWIG 200 [hp_C]  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) 200 [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:50845-0248-1 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 01/30/2019
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/30/2019
    Labeler - Liddell Laboratories, Inc. (832264241)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(50845-0248) , api manufacture(50845-0248) , label(50845-0248) , pack(50845-0248)
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