NDC 50181-0014

Biotox Para

Cochlearia Armoracia, Toxoplasma Gondii, Vibrio Cholerae, Candida Albicans, Trichinella Spiralis

Biotox Para is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by The Wellness Center. The primary component is Horseradish; Toxoplasma Gondii; Vibrio Cholerae; Candida Albicans; Trichinella Spiralis; Taraxacum Officinale; Plasmodium Malariae; Trichophyton Rubrum.

Product ID50181-0014_c8cb0d0d-e9cc-4693-810d-5e24caf782cc
NDC50181-0014
Product TypeHuman Otc Drug
Proprietary NameBiotox Para
Generic NameCochlearia Armoracia, Toxoplasma Gondii, Vibrio Cholerae, Candida Albicans, Trichinella Spiralis
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2013-06-07
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameThe Wellness Center
Substance NameHORSERADISH; TOXOPLASMA GONDII; VIBRIO CHOLERAE; CANDIDA ALBICANS; TRICHINELLA SPIRALIS; TARAXACUM OFFICINALE; PLASMODIUM MALARIAE; TRICHOPHYTON RUBRUM
Active Ingredient Strength3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 50181-0014-1

30 mL in 1 BOTTLE, DROPPER (50181-0014-1)
Marketing Start Date2013-06-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50181-0014-1 [50181001401]

Biotox Para LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2013-06-07
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
HORSERADISH3 [hp_X]/mL

OpenFDA Data

SPL SET ID:c20fe036-8c9a-4132-96c3-5b6089128157
Manufacturer
UNII
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.