NDC 61096-1003

AllergEase

Allium Cepa, Apis Mellifica, Aralia Rac, Arundo, Baptisia, Echinacea, Euphrasia, Gelsemium, Histaminum, Lycopodium, Rhus Tox, Sabadilla, Sanguinaria, Urtica Ur.

AllergEase is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Eight And Company L.l.c. The primary component is Onion; Apis Mellifera; Aralia Racemosa Root; Arundo Pliniana Root; Baptisia Tinctoria Root; Echinacea, Unspecified; Euphrasia Stricta; Gelsemium Sempervirens Root; Histamine Dihydrochloride; Lycopodium Clavatum Spore; Toxicodendron Pubescens Leaf; Schoenocaulon Officinale Seed; Sanguinaria Canadensis Root; Urtica Urens.

• Product ID: 61096-1003_74e86c5a-b657-43c8-b4a0-69e64de51927
• NDC: 61096-1003
• Product Type: Human Otc Drug
• Proprietary Name: AllergEase
• Generic Name: Allium Cepa, Apis Mellifica, Aralia Rac, Arundo, Baptisia, Echinacea, Euphrasia, Gelsemium, Histaminum, Lycopodium, Rhus Tox, Sabadilla, Sanguinaria, Urtica Ur.
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2019-02-26
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Eight and Company L.L.C
• Substance Name: ONION; APIS MELLIFERA; ARALIA RACEMOSA ROOT; ARUNDO PLINIANA ROOT; BAPTISIA TINCTORIA ROOT; ECHINACEA, UNSPECIFIED; EUPHRASIA STRICTA; GELSEMIUM SEMPERVIRENS ROOT; HISTAMINE DIHYDROCHLORIDE; LYCOPODIUM CLAVATUM SPORE; TOXICODENDRON PUBESCENS LEAF; SCHOENOCAULON OFFICINALE SEED; SANGUINARIA CANADENSIS ROOT; URTICA URENS
• Active Ingredient Strength: 6 [hp_X]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_C]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_C]/41mL; [hp_X]/41mL; [hp_X]/41mL; [hp_C]/41mL; [hp_X]/41mL; [hp_C]/41mL; [hp_C]/41mL
• NDC Exclude Flag: N
• Listing Certified Through: 2022-12-31

Packaging

NDC 61096-1003-1

1 BOTTLE, SPRAY in 1 CARTON (61096-1003-1) > 41 mL in 1 BOTTLE, SPRAY

• Marketing Start Date: 2019-02-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 61096-1003-1 [61096100301]

AllergEase LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-02-26

Drug Details

Active Ingredients

Ingredient	Strength
ONION	6 [hp_X]/41mL

OpenFDA Data

• SPL SET ID: ec4fae96-ffe3-489c-9ed2-4aaec114c493
• Manufacturer:
  • Eight and Company L.L.C
• UNII:
  • 639KR60Q1Q
  • IHN2NQ5OF9
  • 5EF0HWI5WU
  • C88X29Y479
  • 6IO182RP7A
  • C9642I91WL
  • 3POA0Q644U
  • T90W4582DU
  • 6NAF1689IO
  • 4N9P6CC1DX
  • ZXE7LB03WC
  • 7S82P3R43Z
  • 492225Q21H
  • N9288CD508
• UPC Code:
  • 0361096000313