43857-0607 : Cardiacforce Oral Liquid


NDC: 43857-0607
Labeler: Bioactive Nutritional, Inc.
Product Type: Human OTC Drug
Drug Name: Cardiacforce
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 43857-0607-1: 30 ML IN 1 BOTTLE, DROPPER (43857‑0607‑1)

Active Ingredients:

  • Adonis Vernalis Whole
  • Black Walnut
  • Convallaria Majalis
  • Digitalis
  • Iberis Amara Seed
  • Leonurus Cardiaca Whole
  • Lycopus Virginicus Whole
  • Magnesium Sulfate Heptahydrate
  • Phosphorus
  • Potassium Chlorate

Dosage Strength:

  • 10 [hp_X]/mL
  • 3 [hp_X]/mL
  • 4 [hp_X]/mL
  • 12 [hp_X]/mL
  • 6 [hp_X]/mL
  • 3 [hp_X]/mL
  • 12 [hp_X]/mL
  • 4 [hp_X]/mL
  • 12 [hp_X]/mL
  • 6 [hp_X]/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Calculi Dissolution Agent [EPC]
  • Cell-mediated Immunity [PE]
  • Dietary Proteins [CS]
  • Increased Histamine Release [PE]
  • Increased Large Intestinal Motility [PE]
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]
  • Magnesium Ion Exchange Activity [MoA]
  • Non-Standardized Food Allergenic Extract [EPC]
  • Nut Proteins [EXT]
  • Osmotic Activity [MoA]
  • Osmotic Laxative [EPC]
  • Potassium Compounds [CS]
  • Potassium Salt [EPC]
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

NDC QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.