NDC 68703-108

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

AllergyEase Desert is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Alfalfa; Onion; Ambrosia Artemisiifolia; Cortisone Acetate; Erechtites Hieraciifolius; Conyza Canadensis; Euonymus Atropurpureus Branch Bark/root Bark; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Schoenocaulon Officinale Seed; Datura Stramonium; Elymus Repens Root.

• Product ID: 68703-108_dae22f30-af57-4cf3-aa2d-968f3626f7d0
• NDC: 68703-108
• Product Type: Human Otc Drug
• Proprietary Name: AllergyEase Desert
• Generic Name: 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
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2013-06-28
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies, LLC
• Substance Name: ADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ALFALFA; ONION; AMBROSIA ARTEMISIIFOLIA; CORTISONE ACETATE; ERECHTITES HIERACIIFOLIUS; CONYZA CANADENSIS; EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; DATURA STRAMONIUM; ELYMUS REPENS ROOT
• 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; [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 68703-108-59

59 mL in 1 BOTTLE, GLASS (68703-108-59)

• Marketing Start Date: 2013-06-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-108-59 [68703010859]

AllergyEase Desert SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-28
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

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

OpenFDA Data

• SPL SET ID: 4a05d51b-e373-4e3b-a0f4-5418a03006f6
• Manufacturer:
  • Native Remedies, LLC
• UNII:
  • K0U68Q2TXA
  • C9642I91WL
  • 16D08B0B9N
  • 9W34L2CQ9A
  • 883WKN7W8X
  • G6W4F0V8Z3
  • 6NAF1689IO
  • WJK59V19EW
  • ID3Z1X61WY
  • 451W47IQ8X
  • J17GBZ5VGX
  • YKH834O4BH
  • 3POA0Q644U
  • 3IXW0F6P8W
  • DJO934BRBD
  • E0399OZS9N
  • 660YQ98I10
  • 93PH5Q8M7E
  • 492225Q21H
  • 1L6JHK0ORR
• UPC Code:
  • 0818837010440