NDC 68703-110

AllergyEase Hawaii

Adenosinum Cyclophosphoricum, Adrenalium, Adrenocorticotrophin, Allium Cepa, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Juniperus Virginiana, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Runex Crisp, Sabadilla

AllergyEase Hawaii is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Onion; Cortisone Acetate; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Juniperus Virginiana Twig; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Rumex Crispus Root; Schoenocaulon Officinale Seed.

• Product ID: 68703-110_0617f99f-d07e-4bbc-a999-92dd05e4c44d
• NDC: 68703-110
• Product Type: Human Otc Drug
• Proprietary Name: AllergyEase Hawaii
• Generic Name: Adenosinum Cyclophosphoricum, Adrenalium, Adrenocorticotrophin, Allium Cepa, Cortisone Aceticum, Euphrasia Officinalis, Galphimia Glauca, Histaminum Hydrochloricum, Juniperus Virginiana, Kali Muriaticum, Mucosa Nasalis Suis, Natrum Muriaticum, Rna, Runex Crisp, Sabadilla
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2013-06-07
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies
• Substance Name: ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ONION; CORTISONE ACETATE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; JUNIPERUS VIRGINIANA TWIG; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; RUMEX CRISPUS ROOT; SCHOENOCAULON OFFICINALE SEED
• Active Ingredient Strength: 12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68703-110-59

59 mL in 1 BOTTLE, GLASS (68703-110-59)

• Marketing Start Date: 2013-06-07
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-110-59 [68703011059]

AllergyEase Hawaii SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-07
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ADENOSINE CYCLIC PHOSPHATE	12 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 9135daa0-eacf-412a-b1f1-eef41c6761f6
• Manufacturer:
  • Native Remedies
• UNII:
  • K0U68Q2TXA
  • C9642I91WL
  • ID3Z1X61WY
  • 6NAF1689IO
  • 883WKN7W8X
  • 532BCG080L
  • 9N1RM2S62C
  • 451W47IQ8X
  • YKH834O4BH
  • 3POA0Q644U
  • J17GBZ5VGX
  • E0399OZS9N
  • 93PH5Q8M7E
  • 492225Q21H
  • 660YQ98I10
• UPC Code:
  • 0818837010464