NDC 68703-124

AllergyEase Shellfish and Seafood

Adrenalinum, Belladona, Bromium, Carbo Animalis, Colchicum Autumnale, Colocynthis, Histaminum Hydrochloricum, Hydrstis Canadensis, Kali Carbonicum, Lycopodium Clavatum, Mercuris Solubilis, Pulsatilla, Urtica Urens

AllergyEase Shellfish and Seafood is a Oral Spray in the Human Otc Drug category. It is labeled and distributed by Native Remedies, Llc. The primary component is Epinephrine; Atropa Belladonna; Bromine; Carbo Animalis; Colchicum Autumnale Bulb; Citrullus Colocynthis Fruit Pulp; Histamine Dihydrochloride; Goldenseal; Potassium Carbonate; Lycopodium Clavatum Spore; Mercurius Solubilis; Pulsatilla Vulgaris; Urtica Urens.

• Product ID: 68703-124_b52f36f0-9fed-4191-b7eb-67552b3bf4e4
• NDC: 68703-124
• Product Type: Human Otc Drug
• Proprietary Name: AllergyEase Shellfish and Seafood
• Generic Name: Adrenalinum, Belladona, Bromium, Carbo Animalis, Colchicum Autumnale, Colocynthis, Histaminum Hydrochloricum, Hydrstis Canadensis, Kali Carbonicum, Lycopodium Clavatum, Mercuris Solubilis, Pulsatilla, Urtica Urens
• Dosage Form: Spray
• Route of Administration: ORAL
• Marketing Start Date: 2013-06-13
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Native Remedies, LLC
• Substance Name: EPINEPHRINE; ATROPA BELLADONNA; BROMINE; CARBO ANIMALIS; COLCHICUM AUTUMNALE BULB; CITRULLUS COLOCYNTHIS FRUIT PULP; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; POTASSIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; PULSATILLA VULGARIS; URTICA URENS
• 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 68703-124-59

59 mL in 1 BOTTLE, GLASS (68703-124-59)

• Marketing Start Date: 2013-06-13
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 68703-124-59 [68703012459]

AllergyEase Shellfish and Seafood SPRAY

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-06-13
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
EPINEPHRINE	12 [hp_X]/59mL

OpenFDA Data

• SPL SET ID: f4c34821-8199-4a14-a583-076ccbb8008d
• Manufacturer:
  • Native Remedies, LLC
• UNII:
  • IHN2NQ5OF9
  • 23H32AOH17
  • 3POA0Q644U
  • 993QHL78E6
  • ZW3Z11D0JV
  • C88X29Y479
  • 279O8I0433
  • 324Y4038G2
  • YKH834O4BH
  • WQZ3G9PF0H
  • I76KB35JEV
  • BQN1B9B9HA
  • SBV4XY874G
• UPC Code:
  • 0818837010600