ALLERGYEASE DESERT- 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, triticum repens spray

AllergyEase Desert by

Drug Labeling and Warnings

AllergyEase Desert by is a Homeopathic medication manufactured, distributed, or labeled by Native Remedies, LLC, King Bio. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Relieves allergies common in the U.S. Desert

ACTIVE INGREDIENT

Drug Facts
Active Ingredients: Equal volumes of each ingredient in 12X, 30X, and LM1 potencies: num 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, Triticum repens

INDICATIONS & USAGE

Uses: For temporary relief of symptoms: itchy, watery eyes, sore throat, cough, runny nose, sneezing, congestion, headaches, hoarseness, and fatigue

WARNINGS

Stop use and ask a doctor if symptoms persist or worsen

PREGNANCY OR BREAST FEEDING

If pregnant or breastfeeding, ask a health professional before use

KEEP OUT OF REACH OF CHILDREN

Keep this and all medication out of reach of children

OVERDOSAGE

In case of overdose, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION

Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Use 3 times daily. Use additionally as needed. Adults: 3 pump sprays. Children 2-12: 2 pump sprays

INACTIVE INGREDIENT

Inactive Ingredients: Citric acid, potassium sorbate, pure water

INFORMATION FOR PATIENTS

The letters HPUS indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the Unites States

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For  more information, visit us at www.nativeremecies.com

Distributed by
Native Remedies, LLC
6531 Park of Commerce Blvd.
Suit 160
Boca Raton, FL 33487
Phone: 1.877.289.1235
International: 1.561.999.8857

No gluten, artificial flavors, or colorants added

STORAGE AND HANDLING

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ALLERGYEASE DESERT 
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, triticum repens spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 68703-108
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (ADENOSINE CYCLIC 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
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 68703-108-59	59 mL in 1 BOTTLE, GLASS

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/28/2013

Labeler - Native Remedies, LLC (192014186)

Establishment
Name	Address	ID/FEI	Business Operations
King Bio		617901350	manufacture(68703-108) , api manufacture(68703-108)