Mercurius Vivus 21X

Product NDC

48951-7182

11-digit product format

489517182

Labeler code

48951

Product ID

48951-7182_93eed10b-88d6-5599-e053-2a95a90a621d

Type

HUMAN OTC DRUG

Nonproprietary name

Mercurius Vivus 21X

Dosage form

LIQUID

Route

ORAL

Labeler

Uriel Pharmacy Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2009-09-01

Marketing end

0000-00-00

Substance

MERCURY

Active strength

21 [hp_X]/mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record