NDC 50181-0057

BioTox P

Pertussinum

BioTox P is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by The Wellness Center For Research And Education. The primary component is Human Sputum, Bordetella Pertussis Infected.

• Product ID: 50181-0057_24ce3717-7660-4140-b48a-29587e097278
• NDC: 50181-0057
• Product Type: Human Otc Drug
• Proprietary Name: BioTox P
• Generic Name: Pertussinum
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 2018-02-27
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: The Wellness Center For Research and Education
• Substance Name: HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
• Active Ingredient Strength: 15 [hp_C]/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 50181-0057-1

30 mL in 1 BOTTLE, DROPPER (50181-0057-1)

• Marketing Start Date: 2018-02-27
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 50181-0057-1 [50181005701]

BioTox P LIQUID

• Marketing Category: unapproved homeopathic
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-02-27

Drug Details

Active Ingredients

Ingredient	Strength
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	15 [hp_C]/mL

OpenFDA Data

• SPL SET ID: bd1a67b8-035d-4a3e-b74f-9b63de30c834
• Manufacturer:
  • The Wellness Center For Research and Education
• UNII:
  • U364V64HUN
• UPC Code:
  • 0737278067601

NDC Crossover Matching brand name "BioTox P" or generic name "Pertussinum"

NDC	Brand Name	Generic Name
50181-0057	BioTox P	Pertussinum
55714-9011	Pertussinum	Pertussinum