BIOTOX

Product NDC

50181-0042

11-digit product format

501810042

Labeler code

50181

Product ID

50181-0042_bd3acb72-ea71-4ed0-8c07-6b50250ea62c

Type

HUMAN OTC DRUG

Nonproprietary name

Cochlearia Armoracia, Varicella Zoster Nosode, Spleen (Suis), Thymus (Suis), Hepar Suis, Epstein-Barr Virus Nosode, Morbillinum, Meningococcus Nosode, Parotidinum, Rubella Nosode, Poliomyelitis Nosode

Dosage form

LIQUID

Route

ORAL

Labeler

The Wellness Center for Research and Education, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-05-19

Marketing end

0000-00-00

Substance

HORSERADISH; HUMAN HERPESVIRUS 3; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; PORK LIVER; HUMAN HERPESVIRUS 4; MEASLES VIRUS; JAPANESE ENCEPHALITIS VIRUS; MUMPS VIRUS; RUBELLA VIRUS; POLIOVIRUS

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_X]/mL; [hp_C]/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record