50181-0014 : Biotox Para Oral Liquid


NDC50181-0014
Labeler: The Wellness Center
Product Type: Human OTC Drug
Drug Name: Biotox Para
Dosage Form: Oral Liquid
Rev. Date: 


NDC Package Codes:

  • 50181-0014-1: 30 ML IN 1 BOTTLE, DROPPER (50181‑0014‑1)

Active Ingredients:

  • Candida Albicans
  • Horseradish
  • Plasmodium Malariae
  • Taraxacum Officinale
  • Toxoplasma Gondii
  • Trichinella Spiralis
  • Trichophyton Rubrum
  • Vibrio Cholerae

Dosage Strength:

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

Pharmaceutical Classes:

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

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.