BioTox Gut

Product NDC

50181-0035

11-digit product format

501810035

Labeler code

50181

Product ID

50181-0035_6803ba40-83b1-4ef4-a574-155d7e256db8

Type

HUMAN OTC DRUG

Nonproprietary name

Cochlearia Armoracia, Phytolacca Decandra, Chelidonium Majus, Intestinal Mucosa, Spleen, Hepar Bovine, Thymus, Salmonella Enteritidis, Helicobacter Pylori, Nux Vomica, Salmonella Paratyphi, Botulinum

Dosage form

LIQUID

Route

ORAL

Labeler

The Wellness Center for Research and Education, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-01-03

Marketing end

0000-00-00

Substance

HORSERADISH; PHYTOLACCA AMERICANA ROOT; CHELIDONIUM MAJUS; BOS TAURUS INTESTINAL MUCOSA; SUS SCROFA SPLEEN; BEEF LIVER; SUS SCROFA THYMUS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; HELICOBACTER PYLORI; STRYCHNOS NUX-VOMICA SEED; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI; BOTULINUM TOXIN TYPE A

Active strength

3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record