Label: REGIONAL ALLERGIES DESERT U.S.- adenosinum cyclophosphoricum, adrenalinum, adrenocorticotrophin, alfalfa, allium cepa, ambrosia artemisiaefolia, cortisone aceticum, erechtites hieracifolia, erigeron canadensis, euonymus atropurpureus, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali muriaticum, mucosa nasalis suis, natrum muriaticum, rna, sabadilla, stramonium and triticum repens 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 July 6, 2020

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  • ACTIVE INGREDIENT

    Drug Facts___________________________________________________________________________________________________________

    HPUS active ingredients: Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium cepa, Ambrosia artemisiaefolia, Cortisone aceticum, Erechtites hieracifolia, Erigeron canadensis, Euonymus atropurpureus, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali muriaticum, Mucosa nasalis suis, Natrum muriaticum, RNA, Sabadilla, Stramonium and Triticum repens.

  • INDICATIONS & USAGE

    Uses for temporary relief of allergy symptoms commonly experienced in AZ, NM and desert areas of CA, NV, UT.

    • itchy, watery eyes
    • runny nose
    • sneezing
    • sore throat
    • sinus congestion
    • cough
    • stuff nose
    • fatigue
    • itchy, irritated skin
    • hoarseness
    • headache
  • DOSAGE & ADMINISTRATION

    Directions

    • Initially depress pump until primed.
    • Spray one dose directly into mouth.
    • Adults: 3 sprays 3 times per day.
    • Children ages 6-12: 2 sprays 3 times per day.
    • Use additionally as needed, up to 6 times per day.
  • WARNINGS

    Warnings

    Stop use and consult a physician if symptoms worsen or persist for more than 7 days.

    If pregnant or breast-feeding, ask a healthcare professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.

  • INACTIVE INGREDIENT

    Inactive ingredients

    Bio-Energetically Enhanced™ pure
    water, 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, Shagbark
    Hickory (Carya ovata) Bark
    Extract, steviol (Steviol
    glycosides).

  • PURPOSE

    Drug Facts___________________________________________________________________________________________________________

    HPUS active ingredients                                                        Purpose

    Equal volumes of each ingredient in 12X, 30X, and LM1 potencies.

    Adenosinum cyclophosphoricum.........................................headache, runny nose

    Adrenalinum....................................................................hay fever, swollen sinuses, lung congestion

    Adrenocorticorticotrophin..................................................inflammation, congestion, cough

    Alfalfa............................................................................stuffed feeling in ear, headache, eye ache

    Allium cepa.....................................................................hay fever, sinus headache, sneezing

    Ambrosia artemisiaefolia...................................................hay fever, wheezy cough

    Cortisone aceticum...........................................................allergic reaction, irritability

    Erechtites hieracifolia........................................................frontal headache, sore throat

    Erigeron canadensis..........................................................head congestion, burning eyes

    Euonymus atropurpureus...................................................tired feeling, headache, vertigo

    Euphrasia officinalis...........................................................discharge from eyes and nose

    Galphimia glauca...............................................................swollen eyelids, hay fever

    Histaminum hydrochloricum................................................coughing fits, itching throat

    Kali muriaticum.................................................................hoarseness, stuffy nose, nosebleed

    Mucosa nasalis suis............................................................sinus headache, nasal congestion

    Natrum muriaticum............................................................watery eyes, sneezing

    RNA.................................................................................allergic reactions

    Sabadilla..........................................................................sore throat, runny nose, sneezing fits

    Stramonium......................................................................pressure on chest, spasmodic cough, dizziness

    Triticum repens..................................................................runny nose, itching eyes, hacking cough

  • STORAGE AND HANDLING

    Keep carton for complete drug facts
    and product information.

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

    For latest product information
    and instructions, visit
    www.DrKings.com

  • PRINCIPAL DISPLAY PANEL

    ra-desert-9-300-1806R01_2.jpg

  • INGREDIENTS AND APPEARANCE
    REGIONAL ALLERGIES DESERT U.S. 
    adenosinum cyclophosphoricum, adrenalinum, adrenocorticotrophin, alfalfa, allium cepa, ambrosia artemisiaefolia, cortisone aceticum, erechtites hieracifolia, erigeron canadensis, euonymus atropurpureus, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali muriaticum, mucosa nasalis suis, natrum muriaticum, rna, sabadilla, stramonium and triticum repens liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57955-0751
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (ADENOSINE CYCLIC PHOSPHATE - UNII:E0399OZS9N) ADENOSINE CYCLIC PHOSPHATE12 [hp_X]  in 59 mL
    EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH) EPINEPHRINE12 [hp_X]  in 59 mL
    CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA) CORTICOTROPIN12 [hp_X]  in 59 mL
    ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD) ALFALFA12 [hp_X]  in 59 mL
    ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H) ONION12 [hp_X]  in 59 mL
    AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A) AMBROSIA ARTEMISIIFOLIA12 [hp_X]  in 59 mL
    CORTISONE ACETATE (UNII: 883WKN7W8X) (CORTISONE - UNII:V27W9254FZ) CORTISONE ACETATE12 [hp_X]  in 59 mL
    ERECHTITES HIERACIIFOLIUS (UNII: 1L6JHK0ORR) (ERECHTITES HIERACIIFOLIUS - UNII:1L6JHK0ORR) ERECHTITES HIERACIIFOLIUS12 [hp_X]  in 59 mL
    CONYZA CANADENSIS (UNII: 16D08B0B9N) (CONYZA CANADENSIS - UNII:16D08B0B9N) CONYZA CANADENSIS12 [hp_X]  in 59 mL
    EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK (UNII: WJK59V19EW) (EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK - UNII:WJK59V19EW) EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK12 [hp_X]  in 59 mL
    EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL) EUPHRASIA STRICTA12 [hp_X]  in 59 mL
    GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E) GALPHIMIA GLAUCA FLOWERING TOP12 [hp_X]  in 59 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 59 mL
    POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CHLORIDE12 [hp_X]  in 59 mL
    SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY) SUS SCROFA NASAL MUCOSA12 [hp_X]  in 59 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE12 [hp_X]  in 59 mL
    SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX) SACCHAROMYCES CEREVISIAE RNA12 [hp_X]  in 59 mL
    SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO) SCHOENOCAULON OFFICINALE SEED12 [hp_X]  in 59 mL
    DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3) DATURA STRAMONIUM12 [hp_X]  in 59 mL
    ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (ELYMUS REPENS ROOT - UNII:3IXW0F6P8W) ELYMUS REPENS ROOT12 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U)  
    POLY-L-LYSINE (30000-70000 MW) (UNII: 0A1V8JTU2M)  
    CARYA OVATA BARK (UNII: X765CF609L)  
    STEVIOL (UNII: 4741LYX6RT)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57955-0751-21 in 1 CARTON10/02/2019
    159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic10/02/2019
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc.617901350manufacture(57955-0751) , api manufacture(57955-0751)
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