NDC 68703-121

AllergyEase Egg and Meat

Calcarea Carbonica, Causticum, Chloramphenicolum, Colchicum Autumnale, Gambonia, Histaminum Hydrochloricum, Hydrastis Canadensis, Ichthyolum, Lecithin, Ova Tosta, Ovi Gallinae Pellicula, Pulsatilla, Pyrogenium

AllergyEase Egg and Meat is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Oyster Shell Calcium Carbonate, Crude; Causticum; Chloramphenicol; Colchicum Autumnale Bulb; Gamboge; Histamine Dihydrochloride; Goldenseal; Ichthammol; Egg Phospholipids; Egg Shell, Cooked; Egg Shell Membrane; Pulsatilla Vulgaris; Rancid Beef.

• Product ID: 68703-121_2893d162-1459-4532-9676-cbc68b5b2f51
• NDC: 68703-121
• Product Type: Human Otc Drug
• Proprietary Name: AllergyEase Egg and Meat
• Generic Name: Calcarea Carbonica, Causticum, Chloramphenicolum, Colchicum Autumnale, Gambonia, Histaminum Hydrochloricum, Hydrastis Canadensis, Ichthyolum, Lecithin, Ova Tosta, Ovi Gallinae Pellicula, Pulsatilla, Pyrogenium
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2013-06-26
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies, LLC
• Substance Name: OYSTER SHELL CALCIUM CARBONATE, CRUDE; CAUSTICUM; CHLORAMPHENICOL; COLCHICUM AUTUMNALE BULB; GAMBOGE; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; ICHTHAMMOL; EGG PHOSPHOLIPIDS; EGG SHELL, COOKED; EGG SHELL MEMBRANE; PULSATILLA VULGARIS; RANCID BEEF
• 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
• NDC Exclude Flag: E
• Listing Certified Through: 2018-12-31

Packaging

NDC 68703-121-59

59 mL in 1 BOTTLE, GLASS (68703-121-59)

• Marketing Start Date: 2013-06-26
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-121-59 [68703012159]

AllergyEase Egg and Meat SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-26
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
OYSTER SHELL CALCIUM CARBONATE, CRUDE	12 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: 4af0a887-c25a-4997-8f47-7e6e79064b50
• Manufacturer:
  • Native Remedies, LLC
• UNII:
  • DD5FO1WKFU
  • 3POA0Q644U
  • 993QHL78E6
  • ZW3Z11D0JV
  • 1Z74184RGV
  • 7556HJ7587
  • NQ14646378
  • 66974FR9Q1
  • N7QBR4212V
  • I76KB35JEV
  • 2E32821G6I
  • 24HBF856C8
  • 29SUH5R3HU
• UPC Code:
  • 0818837010570