Allergies Foundational Formula

ALLERGIES FOUNDATIONAL FORMULA- adenosinum cyclophosphoricum, adrenocorticotrophin, allium cepa, arsenicum album, cortisone aceticum, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali muriaticum, mucosa nasalis suis, natrum muriaticum, rna, sabadilla liquid
New Sun Inc.

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.

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Directions: Before initial dose depress pump 4-5 times or until primed and spray 1 dose directly in mouth 4 to 6 times daily until symptoms improve.

Adult Dose: 3 Pump Sprays

Child's Dose (2-12): 2 Pump Sprays

Warnings:If symptoms persist or worsen, seek advice of physician. If pregnant or breast-feeding, take only on advice of physician.

Keep out of reach of children.

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

Indications: For temporary relief of allergy symptoms: •sore throat •sneezing, cough •fatigue, congestion •watery, itchy eyes

Supports a healthy, balanced immune system.

Active Ingredients: Adenosinum cyclophosphoricum, Adrenocorticotrophin, Allium cepa, Arsenicum album, Cortisone aceticum, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali muriaticum, Mucosa nasalis suis, Natrum muriaticum, RNA, Sabadilla. Equal volumes of each ingredient in 12X, 24X, LM1 potencies.

Inactive Ingredient: Citric acid, potassium sorbate, purified water.

Indications: For temporary relief of allergy symptoms:

sore throat
sneezing, cough
fatigue, congestion
watery, itchy eyes

Supports a healthy, balanced immune system.

image description

ALLERGIES FOUNDATIONAL FORMULA
adenosinum cyclophosphoricum, adrenocorticotrophin, allium cepa, arsenicum album, cortisone aceticum, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali muriaticum, mucosa nasalis suis, natrum muriaticum, rna, sabadilla liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66579-0065
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ADENOSINE CYCLIC PHOSPHATE (UNII: E0399OZS9N) (ADENOSINE CYCLIC 3',5'-PHOSPHATE - UNII:E0399OZS9N)	ADENOSINE CYCLIC PHOSPHATE	12 [hp_X] in 29 mL
CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA)	CORTICOTROPIN	12 [hp_X] in 29 mL
ONION (UNII: 492225Q21H) (ONION - UNII:492225Q21H)	ONION	12 [hp_X] in 29 mL
ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV)	ARSENIC TRIOXIDE	12 [hp_X] in 29 mL
CORTISONE ACETATE (UNII: 883WKN7W8X) (CORTISONE - UNII:V27W9254FZ)	CORTISONE ACETATE	12 [hp_X] in 29 mL
EUPHRASIA STRICTA (UNII: C9642I91WL) (EUPHRASIA STRICTA - UNII:C9642I91WL)	EUPHRASIA STRICTA	12 [hp_X] in 29 mL
GALPHIMIA GLAUCA FLOWERING TOP (UNII: 93PH5Q8M7E) (GALPHIMIA GLAUCA FLOWERING TOP - UNII:93PH5Q8M7E)	GALPHIMIA GLAUCA FLOWERING TOP	12 [hp_X] in 29 mL
HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3)	HISTAMINE DIHYDROCHLORIDE	12 [hp_X] in 29 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10) (POTASSIUM CATION - UNII:295O53K152)	POTASSIUM CATION	12 [hp_X] in 29 mL
SUS SCROFA NASAL MUCOSA (UNII: ID3Z1X61WY) (SUS SCROFA NASAL MUCOSA - UNII:ID3Z1X61WY)	SUS SCROFA NASAL MUCOSA	12 [hp_X] in 29 mL
SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	SODIUM CHLORIDE	12 [hp_X] in 29 mL
SACCHAROMYCES CEREVISIAE RNA (UNII: J17GBZ5VGX) (SACCHAROMYCES CEREVISIAE RNA - UNII:J17GBZ5VGX)	SACCHAROMYCES CEREVISIAE RNA	12 [hp_X] in 29 mL
SCHOENOCAULON OFFICINALE SEED (UNII: 6NAF1689IO) (SCHOENOCAULON OFFICINALE SEED - UNII:6NAF1689IO)	SCHOENOCAULON OFFICINALE SEED	12 [hp_X] in 29 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66579-0065-1	29 mL in 1 BOTTLE, SPRAY

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		07/16/2014

Labeler - New Sun Inc. (957251176)

Registrant - New Sun Inc. (957251176)