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

Allergies Foundational Formula by

Drug Labeling and Warnings

Allergies Foundational Formula by is a Homeopathic medication manufactured, distributed, or labeled by New Sun Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

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

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

Keep out of reach of children.

OTHER SAFETY INFORMATION

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

PURPOSE

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

Supports a healthy, balanced immune system.

ACTIVE INGREDIENT

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

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

INDICATIONS & USAGE

Indications: For temporary relief of allergy symptoms:

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

Supports a healthy, balanced immune system.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

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

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 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

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: 66579-0065-1	29 mL in 1 BOTTLE, SPRAY

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

Labeler - New Sun Inc. (957251176)

Registrant - New Sun Inc. (957251176)