50181-0035 : Biotox Gut Oral Liquid


NDC: 50181-0035
Labeler: The Wellness Center for Research and Education, Inc.
Product Type: Human OTC Drug
Drug Name: Biotox Gut
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 50181-0035-1: 30 ML IN 1 BOTTLE, DROPPER (50181‑0035‑1)

Active Ingredients:

  • Beef Liver
  • Bos Taurus Intestinal Mucosa
  • Botulinum Toxin Type a
  • Chelidonium Majus Whole
  • Helicobacter Pylori
  • Horseradish
  • Phytolacca Americana Root
  • Salmonella Enterica Subsp. Enterica Serovar Enteritidis
  • Salmonella Enterica Subsp. Enterica Serovar Typhi
  • Strychnos Nux-vomica Seed
  • Sus Scrofa Spleen
  • Sus Scrofa Thymus

Dosage Strength:

  • 8 [hp_X]/mL
  • 8 [hp_X]/mL
  • 30 [hp_C]/mL
  • 3 [hp_X]/mL
  • 15 [hp_X]/mL
  • 3 [hp_X]/mL
  • 3 [hp_X]/mL
  • 12 [hp_X]/mL
  • 15 [hp_C]/mL
  • 3 [hp_C]/mL
  • 8 [hp_X]/mL
  • 8 [hp_X]/mL

Pharmaceutical Classes:

  • Acetylcholine Release Inhibitor [EPC]
  • Acetylcholine Release Inhibitors [MoA]
  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Dietary Proteins [CS]
  • Food Additives [CS]
  • Increased Histamine Release [PE]
  • Increased IgG Production [PE]
  • Meat Proteins [EXT]
  • Neuromuscular Blockade [PE]
  • Neuromuscular Blocker [EPC]
  • Non-Standardized Food Allergenic Extract [EPC]
  • Non-Standardized Plant Allergenic Extract [EPC]
  • Plant Proteins [CS]
  • Seed Storage Proteins [CS]

NDC QR Code

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NDC 50181-0035 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.