Label: ALLERGY RELIEF NOW HAY FEVER REMEDY- onion, ambrosia artemisiifolia, arsenic triiodide, bromine, euphrasia stricta, gelsemium sempervirens root, sodium chloride, schoenocaulon officinale seed, sanguinaria canadensis root and histamine dihydrochloride spray

  • NDC Code(s): 61727-053-30
  • Packager: Homeocare Laboratories
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved homeopathic

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 03/14

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  • Active Ingredients:

    Allium Cepa 6X, Ambrosia 6X, Arsenicum Iodatum 10X, Bromium 10X, Euphrasia Officinalis 6X, Gelsemium Sempervirens 6X, Natrum Muriaticum 10X, Sabadilla 6X, Sanguinaria Canadensis 6X, Histaminum Hydrochloricum 12X

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  • Inactive Ingredients:

    Purified Water, Alcohol USP 20%

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  • Suggested Usage:

    Adults spray three times per day under tongue. Children age 12 and under spray one time per day under tongue. Store in a cool dry place.

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  • INDICATIONS & USAGE

    For grass and tree pollen ​Homeopathic Spray

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children

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  • WARNINGS

    Do not use if outer seal is missing

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  • Allergy Now Hay Fever Remedy 1 fl oz

    Concordia_LabelFinal-hayfever.pdfAllergy Now Hay Fever Remedy

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  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF NOW HAY FEVER REMEDY 
    hay fever remedy spray
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:61727-053
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ONION (ONION) ONION 6 [hp_X]  in 1 [hp_X]
    AMBROSIA ARTEMISIIFOLIA (AMBROSIA ARTEMISIIFOLIA) AMBROSIA ARTEMISIIFOLIA 6 [hp_X]  in 1 [hp_X]
    ARSENIC TRIIODIDE (ARSENIC CATION (3+)) ARSENIC CATION (3+) 10 [hp_X]  in 1 [hp_X]
    bromine (BROMINE) bromine 10 [hp_X]  in 1 [hp_X]
    EUPHRASIA STRICTA (EUPHRASIA STRICTA) EUPHRASIA STRICTA 6 [hp_X]  in 1 [hp_X]
    GELSEMIUM SEMPERVIRENS ROOT (GELSEMIUM SEMPERVIRENS ROOT) GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]  in 1 [hp_X]
    SODIUM CHLORIDE (CHLORIDE ION) SODIUM CHLORIDE 10 [hp_X]  in 1 [hp_X]
    SCHOENOCAULON OFFICINALE SEED (SCHOENOCAULON OFFICINALE SEED) SCHOENOCAULON OFFICINALE SEED 6 [hp_X]  in 1 [hp_X]
    SANGUINARIA CANADENSIS ROOT (SANGUINARIA CANADENSIS ROOT) SANGUINARIA CANADENSIS ROOT 6 [hp_X]  in 1 [hp_X]
    HISTAMINE DIHYDROCHLORIDE (HISTAMINE) HISTAMINE DIHYDROCHLORIDE 12 [hp_X]  in 1 [hp_X]
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    ALCOHOL  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:61727-053-30 1 [hp_X] in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 03/25/2014
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    Name Address ID/FEI Business Operations
    Homeocare Laboratories 088248828 manufacture(61727-053)
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