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

Regional Allergies Desert U.S. by

Drug Labeling and Warnings

Regional Allergies Desert U.S. by is a Homeopathic medication manufactured, distributed, or labeled by King Bio Inc., KingBio Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

WARNINGS

Warnings

• If symptoms persist more than seven days or worsen, consult a physician.
• If pregnant or breast-feeding, ask a healthcare professional before use.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

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.

OTHER SAFETY INFORMATION

Other information

Tamper resistant for your protection. Use only if safety seal is intact.

INACTIVE INGREDIENT

Inactive ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

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

PRINCIPAL DISPLAY PANEL

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 Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57955-8195
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (ADENOSINE CYCLIC 3',5'-PHOSPHATE - UNII:E0399OZS9N)	ADENOSINE CYCLIC PHOSPHATE	12 [hp_X]  in 59 mL
EPINEPHRINE (UNII: YKH834O4BH) (EPINEPHRINE - UNII:YKH834O4BH)	EPINEPHRINE	12 [hp_X]  in 59 mL
CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA)	CORTICOTROPIN	12 [hp_X]  in 59 mL
ALFALFA (UNII: DJO934BRBD) (ALFALFA - UNII:DJO934BRBD)	ALFALFA	12 [hp_X]  in 59 mL
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	12 [hp_X]  in 59 mL
AMBROSIA ARTEMISIIFOLIA (UNII: 9W34L2CQ9A) (AMBROSIA ARTEMISIIFOLIA - UNII:9W34L2CQ9A)	AMBROSIA ARTEMISIIFOLIA	12 [hp_X]  in 59 mL
CORTISONE ACETATE (UNII: 883WKN7W8X) (CORTISONE - UNII:V27W9254FZ)	CORTISONE ACETATE	12 [hp_X]  in 59 mL
ERECHTITES HIERACIIFOLIUS (UNII: 1L6JHK0ORR) (ERECHTITES HIERACIIFOLIUS - UNII:1L6JHK0ORR)	ERECHTITES HIERACIIFOLIUS	12 [hp_X]  in 59 mL
CONYZA CANADENSIS (UNII: 16D08B0B9N) (CONYZA CANADENSIS - UNII:16D08B0B9N)	CONYZA CANADENSIS	12 [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 BARK	12 [hp_X]  in 59 mL
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	12 [hp_X]  in 59 mL
GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E)	GALPHIMIA GLAUCA FLOWERING TOP	12 [hp_X]  in 59 mL
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	12 [hp_X]  in 59 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CHLORIDE	12 [hp_X]  in 59 mL
SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY)	SUS SCROFA NASAL MUCOSA	12 [hp_X]  in 59 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	12 [hp_X]  in 59 mL
SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX)	SACCHAROMYCES CEREVISIAE RNA	12 [hp_X]  in 59 mL
SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO)	SCHOENOCAULON OFFICINALE SEED	12 [hp_X]  in 59 mL
DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (DATURA STRAMONIUM - UNII:G6W4F0V8Z3)	DATURA STRAMONIUM	12 [hp_X]  in 59 mL
ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (ELYMUS REPENS ROOT - UNII:3IXW0F6P8W)	ELYMUS REPENS ROOT	12 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57955-8195-2	59 mL in 1 BOTTLE, SPRAY

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		07/09/2013

Labeler - King Bio Inc. (617901350)

Registrant - King Bio Inc. (617901350)

Establishment
Name	Address	ID/FEI	Business Operations
KingBio Inc.		617901350	api manufacture(57955-8195)