50181-0078 : Biotox Bac Oral Liquid


NDC: 50181-0078
Labeler: The Wellness Center for Research and Education, Inc.
Product Type: Human OTC Drug
Drug Name: Biotox Bac 3
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 50181-0078-1: 30 ML IN 1 BOTTLE, DROPPER (50181‑0078‑1)

Active Ingredients:

  • Mycoplasma Pneumoniae
  • Proteus Inconstans
  • Candida Albicans
  • Escherichia Coli
  • Mycobacterium Avium Subsp. Paratuberculosis
  • Pasteurella Multocida
  • Streptococcus Pneumoniae
  • Thuja Occidentalis Leafy Twig
  • Phytolacca Americana Root
  • Legionella Pneumophila
  • Shigella Sonnei

Dosage Strength:

  • 9 [hp_X]/mL
  • 12 [hp_X]/mL
  • 15 [hp_X]/mL
  • 15 [hp_X]/mL
  • 15 [hp_X]/mL
  • 15 [hp_X]/mL
  • 15 [hp_X]/mL
  • 15 [hp_X]/mL
  • 6 [hp_C]/mL
  • 15 [hp_C]/mL
  • 15 [hp_C]/mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Fungal Proteins [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Non-Standardized Fungal Allergenic Extract [EPC]

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.