Label: ALLERGY HAY FEVER RELIEVER- allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, naphthalinum, natrum muriaticum, sabadilla, wyethia helenioides liquid

  • 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 September 2, 2022

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

  • Warnings

    Stop use and ask your doctor if symptoms
    persist or worsen.

    If pregnant or breast-feeding, take only on
    advice of a healthcare professional.

    Keep out of reach of children.

    Reference image: Hay fever.jpg

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

    Reference imageHay fever.jpg

  • Directions

    Initially, depress pump until
    primed. Spray one dose directly into mouth.

    Adults: 3 sprays 3 times per day.

    Children (6 - 12): 2 sprays 3 times per day.

    Consult a physician for use in children
    under 6 years of age.

    Use additionally as
    needed, up to 6 times per day.

    Reference image: Hay fever.jpg

  • OTHER SAFETY INFORMATION

    Tamper resistant for your protection. Use
    only if seal is intact. This product has not been
    clinically tested.

    King Bio, Inc. FDA Reg. #1053442
    3 Westside Dr. Asheville, NC 28806 USA
    Questions? Call 866.298.2740

    Reference image: Hay fever.jpg

  • Active ingredients

    Allium cepa, Ambrosia
    artemisiaefolia, Arsenicum album, Arum
    triphyllum, Arundo mauritanica, Euphrasia
    officinalis, Naphthalinum, Natrum muriaticum,
    Sabadilla, Wyethia helenioides. Equal volumes of
    each HPUS ingredient in 10X, 30X, 100X, 1LM,
    2LM, 3LM, 5LM potencies.

    Reference image: Hay fever.jpg 

  • Uses

    For temporary relief of allergy and hay
    fever symptoms: nasal and sinus congestion,
    runny nose, sneezing, coughing, watery eyes.

    Reference image: Hay fever.jpg

  • Inactive ingredients

    Citrus Extract (ascorbic
    acid, citric acid, citrus aurantium amara fruit
    extract, citrus aurantium sinensis peel extract,
    citrus reticulata fruit extract, demineralized water,
    glycerin, lactic acid), Honeysuckle (Lonicera
    japonica), Polylysine, Purified Water, Shagbark
    Hickory (Carya ovata) Bark Extract, Steviol
    (Steviol glycosides).

    Reference image: Hay fever.jpg

  • PURPOSE

    For temporary relief of allergy and hay fever symptoms:

    nasal and sinus congestion

    runny nose

    sneezing

    coughing

    watery eyes

    Reference image: Hay fever.jpg

  • PRINCIPAL DISPLAY PANEL

    image description Hay fever.jpg

  • INGREDIENTS AND APPEARANCE
    ALLERGY HAY FEVER RELIEVER 
    allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, naphthalinum, natrum muriaticum, sabadilla, wyethia helenioides liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57955-9002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION10 [hp_X]  in 59 mL
    AMBROSIA ARTEMISIIFOLIA WHOLE (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA WHOLE10 [hp_X]  in 59 mL
    ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE10 [hp_X]  in 59 mL
    ARISAEMA TRIPHYLLUM ROOT (UNII: DM64K844DM) (ARISAEMA TRIPHYLLUM ROOT - UNII:DM64K844DM) ARISAEMA TRIPHYLLUM ROOT10 [hp_X]  in 59 mL
    ARUNDO PLINIANA ROOT (UNII: ZXE7LB03WC) (ARUNDO PLINIANA ROOT - UNII:ZXE7LB03WC) ARUNDO PLINIANA ROOT10 [hp_X]  in 59 mL
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA10 [hp_X]  in 59 mL
    NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE10 [hp_X]  in 59 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE10 [hp_X]  in 59 mL
    SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED10 [hp_X]  in 59 mL
    WYETHIA HELENIOIDES ROOT (UNII: J10PD1AQ0N) (WYETHIA HELENIOIDES ROOT - UNII:J10PD1AQ0N) WYETHIA HELENIOIDES ROOT10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    CITRUS AURANTIUM FRUIT OIL (UNII: 59JDQ5VT0T)  
    ORANGE PEEL (UNII: TI9T76XD44)  
    CITRUS RETICULATA FRUIT OIL (UNII: 25P9H3QU5E)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)  
    BENZYLPENICILLOYL POLYLYSINE (UNII: 76479814OY)  
    CARYA OVATA BARK (UNII: X765CF609L)  
    STEVIOL (UNII: 4741LYX6RT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57955-9002-259 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/22/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic04/22/2022
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc.617901350manufacture(57955-9002) , api manufacture(57955-9002)