57520-0612 : Scrofularoforce Oral Liquid


NDC: 57520-0612
Labeler: Apotheca Company
Product Type: Human OTC Drug
Drug Name: Scrofularoforce
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 57520-0612-1: 30 ML IN 1 BOTTLE, DROPPER (57520‑0612‑1)

Active Ingredients:

  • Atropa Belladonna
  • Barium Carbonate
  • Barium Chloride Dihydrate
  • Conium Maculatum Flowering Top
  • Helleborus Niger Root
  • Iodine
  • Juniperus Virginiana Twig
  • Lachesis Muta Venom
  • Oyster Shell Calcium Carbonate
  • Crude
  • Potassium Phosphate
  • Dibasic
  • Rumex Crispus Root
  • Scrophularia Nodosa
  • Silicon Dioxide
  • Sodium Phosphate
  • Dibasic Anhydrous
  • Sus Scrofa Lymph
  • Zanthoxylum Americanum Bark

Dosage Strength:

  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 3 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 12 [hp_X]/mL
  • 12 [hp_X]/mL
  • 8 [hp_X]/mL
  • 3 [hp_X]/mL

Related Products:

Based on records with the same trade name.
  • 43857-0062 Scrofularoforce Oral Liquid by Bioactive Nutritional, Inc.
  • 43857-0479 Scrofularoforce Oral Liquid by Bioactive Nutritional, Inc.
  • 43857-0580 Scrofularoforce Oral Liquid by Bioactive Nutritional, Inc.

NDC QR Code

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NDC 57520-0612 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.