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Earache (Liddell Laboratories, Inc.)

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SPRAY 30 mL in 1 BOTTLE, SPRAY (50845-0119-1) Label Information

Complete Earache Information

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS:  Aconitum napellus 200C, Anthracinum 200C, Arnica montana 200C, Bapisia tinctoria 3X, Capsicum annuum 6X, Chamomilla 3X, Chenopodium anthelminticum 4X, Euphorbium officinarum 4X, Lachesis mutus 200C, Magnesia phosphorica 8X, Mercurius corrosivus 200C, Plantago major 3X, Pulsatilla 30X, Verbascum thapsus 3X.



  • PURPOSE

    INDICATIONS:  Temporarily relieves symptoms associated with earache:  pain, inflammation, discharge, burning sensation.



  • WARNINGS

    WARNINGS:  If symptoms persist, consult a doctor.

    If pregnant or breast feeding, ask a doctor before use.

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

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



  • DOSAGE & ADMINISTRATION

    DIRECTIONS:  Adults and children over 12:  Place 15 drops under the tongue up to 6 times per day until symptoms are relieved.

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


  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:  Organic alcohol 20% v/v, Purified water.



  • 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.


  • INDICATIONS & USAGE

    INDICATIONS:  Temporarily relieves symptoms associated with earache: pain, inflammation, discharge, burning sensation.



  • QUESTIONS

    LIDDELL LABORATORIES

    WOODBINE, IA 51579

    WWW.LIDDELL.NET

    1-800-460-7733


  • PRINCIPAL DISPLAY PANEL

    ORAL SPRAYS

    LIDDELL LABORATORIES

    26

    Ear

    Earache

    HOMEOPATHIC

    1.0 FL. OZ. (30 ml)

    Earache


  • INGREDIENTS AND APPEARANCE
    EARACHE 
    aconitum napellus, anthracinum, arnica montana, baptisia tinctoria, capsicum annuum, chamomilla, chenopodium anthelminticum, euphorbium officinarum, lachesis mutus, magnesia phosphorica, spray
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:50845-0119
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ACONITUM NAPELLUS (UNII: U0NQ8555JD) (ACONITUM NAPELLUS - UNII:U0NQ8555JD) ACONITUM NAPELLUS 200 [hp_C]  in 1 mL
    BACILLUS ANTHRACIS IMMUNOSERUM RABBIT (UNII: 41LZ22DD4N) (BACILLUS ANTHRACIS IMMUNOSERUM RABBIT - UNII:41LZ22DD4N) BACILLUS ANTHRACIS IMMUNOSERUM RABBIT 200 [hp_C]  in 1 mL
    ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW) ARNICA MONTANA 200 [hp_C]  in 1 mL
    BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (BAPTISIA TINCTORIA ROOT - UNII:5EF0HWI5WU) BAPTISIA TINCTORIA ROOT 3 [hp_X]  in 1 mL
    CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG) CAPSICUM 6 [hp_X]  in 1 mL
    CHAMOMILE (UNII: FGL3685T2X) (CHAMOMILE - UNII:FGL3685T2X) CHAMOMILE 3 [hp_X]  in 1 mL
    CHENOPODIUM AMBROSIOIDES (UNII: 4H5RSU087I) (CHENOPODIUM AMBROSIOIDES - UNII:4H5RSU087I) CHENOPODIUM AMBROSIOIDES 4 [hp_X]  in 1 mL
    EUPHORBIA RESINIFERA RESIN (UNII: 1TI1O9028K) (EUPHORBIA RESINIFERA RESIN - UNII:1TI1O9028K) EUPHORBIA RESINIFERA RESIN 4 [hp_X]  in 1 mL
    LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I) LACHESIS MUTA VENOM 200 [hp_C]  in 1 mL
    MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE (UNII: HF539G9L3Q) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 8 [hp_X]  in 1 mL
    MERCURIC CHLORIDE (UNII: 53GH7MZT1R) (MERCURIC CATION - UNII:ED30FJ8Y42) MERCURIC CHLORIDE 200 [hp_C]  in 1 mL
    PLANTAGO MAJOR (UNII: W2469WNO6U) (PLANTAGO MAJOR - UNII:W2469WNO6U) PLANTAGO MAJOR 3 [hp_X]  in 1 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 30 [hp_X]  in 1 mL
    VERBASCUM THAPSUS (UNII: C9TD27U172) (VERBASCUM THAPSUS - UNII:C9TD27U172) VERBASCUM THAPSUS 3 [hp_X]  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:50845-0119-1 30 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 01/25/2011
    Labeler - Liddell Laboratories, Inc. (832264241)
    Establishment
    Name Address ID/FEI Business Operations
    Liddell Laboratories, Inc. 832264241 manufacture