Promolaxin

Product NDC

35356-822

11-digit product format

353560822

Labeler code

35356

Product ID

35356-822_2f91cc14-feaf-4dfb-ad6d-abb61c711c88

Type

HUMAN OTC DRUG

Nonproprietary name

Docusate sodium

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

part334

Marketing category

OTC MONOGRAPH NOT FINAL

Marketing start

2011-04-15

Marketing end

0000-00-00

Substance

DOCUSATE SODIUM

Active strength

100 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record