ALLERGY / HAY FEVER RWELIEVER- onion, ambrosia artemisiifolia, arsenic trioxide, arisaema triphyllum root, arundo pliniana root, euphrasia stricta, naphthalene, sodium chloride, schoenocaulon officinale seed and wyethia helenioides root 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.

----------

Allergy Hay Fever Reliever

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

Infants - 2 yrs. 1 Pump Spray

Warnings: If symptoms persist or worsen, seek advice of a 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: • head and nasal congestion • mucus discharge • sneezing • cough • hoarseness • sore throat • red, itchy, or watery eyes • sensitivity to light • dry mucus membranes or lips.

Active Ingredients: ​Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Naphthalinum, Natrum muriaticum, Sabadilla, Wyethia helenioides. ​Equal volumes of each ingredient in 10X, 30X, and 100X potencies.

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

Indications: For temporary relief of:

  • head and nasal congestion
  • mucus discharge
  • sneezing
  • cough
  • hoarseness
  • sore throat
  • red, itchy, or watery eyes
  • sensitivity to light
  • dry mucus membranes or lips

image description

ALLERGY / HAY FEVER RWELIEVER 
allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, naphthalinum, natrum muriaticum, sabadilla, wyethia helenioides liquid
Product Information
Product TypeHUMAN OTC DRUG LABELItem Code (Source)NDC:66579-0011
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ONION (ONION) ONION10 [hp_X]  in 59 mL
AMBROSIA ARTEMISIIFOLIA (AMBROSIA ARTEMISIIFOLIA) AMBROSIA ARTEMISIIFOLIA10 [hp_X]  in 59 mL
ARSENIC TRIOXIDE (ARSENIC CATION (3+)) ARSENIC TRIOXIDE10 [hp_X]  in 59 mL
ARISAEMA TRIPHYLLUM ROOT (ARISAEMA TRIPHYLLUM ROOT) ARISAEMA TRIPHYLLUM ROOT10 [hp_X]  in 59 mL
ARUNDO PLINIANA ROOT (ARUNDO PLINIANA ROOT) ARUNDO PLINIANA ROOT10 [hp_X]  in 59 mL
EUPHRASIA STRICTA (EUPHRASIA STRICTA) EUPHRASIA STRICTA10 [hp_X]  in 59 mL
NAPHTHALENE (NAPHTHALENE) NAPHTHALENE10 [hp_X]  in 59 mL
SODIUM CHLORIDE (CHLORIDE ION) SODIUM CHLORIDE10 [hp_X]  in 59 mL
SCHOENOCAULON OFFICINALE SEED (SCHOENOCAULON OFFICINALE SEED) SCHOENOCAULON OFFICINALE SEED10 [hp_X]  in 59 mL
WYETHIA HELENIOIDES ROOT (WYETHIA HELENIOIDES ROOT) WYETHIA HELENIOIDES ROOT10 [hp_X]  in 59 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE 
POTASSIUM SORBATE 
WATER 
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66579-0011-229 mL in 1 BOTTLE, SPRAY
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic09/08/2014
Labeler - New Sun Inc. (957251176)
Registrant - New Sun Inc. (957251176)

Revised: 9/2014
Document Id: f6ed253e-cd39-41da-a6d5-2563d0ac491f
Set id: 34f6f683-78c9-4d4b-beee-4f3f3f438292
Version: 1
Effective Time: 20140908
 
New Sun Inc.