Label: ALLERGY RELIEF NOW HAY FEVER REMEDY- hay fever remedy spray

  • NDC Code(s): 61727-053-30
  • Packager: Homeocare Laboratories
  • Category: HUMAN OTC DRUG LABEL

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 March 25, 2014

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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

  • Inactive Ingredients:

    Purified Water, Alcohol USP 20%

  • 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.

  • PURPOSE

  • INDICATIONS & USAGE

    For grass and tree pollen ​Homeopathic Spray

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children

  • WARNINGS

    Do not use if outer seal is missing

  • Allergy Now Hay Fever Remedy 1 fl oz

    Concordia_LabelFinal-hayfever.pdfAllergy Now Hay Fever Remedy

  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF NOW HAY FEVER REMEDY 
    hay fever remedy spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61727-053
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION6 [hp_X]  in 1 [hp_X]
    AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA6 [hp_X]  in 1 [hp_X]
    ARSENIC TRIIODIDE (UNII: 3029988O2T) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC CATION (3+)10 [hp_X]  in 1 [hp_X]
    bromine (UNII: SBV4XY874G) (BROMINE - UNII:SBV4XY874G) bromine10 [hp_X]  in 1 [hp_X]
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA6 [hp_X]  in 1 [hp_X]
    GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (GELSEMIUM SEMPERVIRENS ROOT - UNII:639KR60Q1Q) GELSEMIUM SEMPERVIRENS ROOT6 [hp_X]  in 1 [hp_X]
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE10 [hp_X]  in 1 [hp_X]
    SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED6 [hp_X]  in 1 [hp_X]
    SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) (SANGUINARIA CANADENSIS ROOT - UNII:N9288CD508) SANGUINARIA CANADENSIS ROOT6 [hp_X]  in 1 [hp_X]
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 1 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:61727-053-301 [hp_X] in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/25/2014
    Labeler - Homeocare Laboratories (088248828)
    Registrant - Homeocare Laboratories (088248828)
    Establishment
    NameAddressID/FEIBusiness Operations
    Homeocare Laboratories088248828manufacture(61727-053)
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