Drugplain

Mucus Relief PE 400 mg/1

Guaifenesin, Phenylephrine HCl · TABLET, FILM COATED · Walgreen Company

No Recall History
Plain English

Mucus Relief PE is a tablet, film coated containing guaifenesin, phenylephrine hcl at 400 mg/1, taken oral. Manufactured by Walgreen Company.

Key Facts

Brand Name
Mucus Relief PE
Generic Name
Guaifenesin, Phenylephrine HCl
NDC Code (Product)
0363-0542
Manufacturer
Walgreen Company
Strength
400 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
M012
Drug Class
Expectorant [EPC]
Marketing Start
04/15/2006

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

acute kidney injury2 reports
chronic kidney disease2 reports
infection2 reports
infusion related reaction2 reports
neuropathy peripheral2 reports
pain2 reports
rash2 reports
tinnitus2 reports
abdominal pain upper1 reports
alopecia1 reports

Frequently Asked Questions

What is Mucus Relief PE used for?

Mucus Relief PE contains Guaifenesin, Phenylephrine HCl. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Mucus Relief PE a controlled substance?

Mucus Relief PE is not classified as a controlled substance by the DEA.

What is the generic name for Mucus Relief PE?

The generic name for Mucus Relief PE is Guaifenesin, Phenylephrine HCl. There are 8 other brand versions of Guaifenesin, Phenylephrine HCl.

What is the NDC code for Mucus Relief PE 400 mg/1?

The NDC (National Drug Code) for Mucus Relief PE 400 mg/1 is 0363-0542, listed by Walgreen Company.