Toxoplasma Gondii Remedy

Product NDC

43742-0340

11-digit product format

437420340

Labeler code

43742

Product ID

43742-0340_25d5ae9a-5298-45c7-abd9-0390170e5136

Type

HUMAN OTC DRUG

Nonproprietary name

Toxoplasma Gondii

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2014-07-15

Marketing end

2020-12-14

Substance

TOXOPLASMA GONDII

Active strength

15 [hp_X]/mL

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record