NDC 52731-7005

Respiratory Complex

Antimonium Tartaricum, Bryonia, Chelidonium Majus, Echinacea Angustifolia, Hepar Sulphuris Calcareum, Hepatica Tribola, Lycopodium Clavatum, Phosphorus, Stannum Metallicum, Sticta Pulmonaria

Respiratory Complex is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Nova Homeopathic Therapeutics, Inc.. The primary component is Antimony Potassium Tartrate; Bryonia Alba Root; Chelidonium Majus; Echinacea Angustifolia; Calcium Sulfide; Hepatica Nobilis Var. Obtusa; Lycopodium Clavatum Spore; Phosphorus; Tin; Lobaria Pulmonaria.

• Product ID: 52731-7005_b5118f88-1dcd-4dc7-9488-3a1cff4bb584
• NDC: 52731-7005
• Product Type: Human Otc Drug
• Proprietary Name: Respiratory Complex
• Generic Name: Antimonium Tartaricum, Bryonia, Chelidonium Majus, Echinacea Angustifolia, Hepar Sulphuris Calcareum, Hepatica Tribola, Lycopodium Clavatum, Phosphorus, Stannum Metallicum, Sticta Pulmonaria
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2011-06-01
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: Nova Homeopathic Therapeutics, Inc.
• Substance Name: ANTIMONY POTASSIUM TARTRATE; BRYONIA ALBA ROOT; CHELIDONIUM MAJUS; ECHINACEA ANGUSTIFOLIA; CALCIUM SULFIDE; HEPATICA NOBILIS VAR. OBTUSA; LYCOPODIUM CLAVATUM SPORE; PHOSPHORUS; TIN; LOBARIA PULMONARIA
• Active Ingredient Strength: 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 52731-7005-2

1 BOTTLE in 1 BOX (52731-7005-2) > 50 mL in 1 BOTTLE (52731-7005-1)

• Marketing Start Date: 2011-06-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 52731-7005-1 [52731700501]

Respiratory Complex LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-06-01

NDC 52731-7005-2 [52731700502]

Respiratory Complex LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-06-01
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
ANTIMONY POTASSIUM TARTRATE	6 [hp_X]/mL

OpenFDA Data

• SPL SET ID: 66184d48-4b25-4339-bfdd-6ba17f554d31
• Manufacturer:
  • Nova Homeopathic Therapeutics, Inc.
• UNII:
  • D1YM0P5Z2T
  • T7J046YI2B
  • C88X29Y479
  • 7E889U5RNN
  • DL6OZ476V3
  • 387GMG9FH5
  • 6ICN6T7FEM
  • 27YLU75U4W
  • 1MBW07J51Q
  • VB06AV5US8
• UPC Code:
  • 0045946070052