Active Ingredient
(in each extended-release tablet)
Guaifenesin USP 1200 mg
The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid Corporation for the product Guaifenesin (NDC 11822-4260). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, ask a doctor before use if you have, stop use and ask a doctor if, if pregnant or breast-feeding,, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(in each extended-release tablet)
Guaifenesin USP 1200 mg
Expectorant
Do not use
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
colloidal silicon dioxide, hypromellose, magnesium stearate, microcrystalline cellulose, povidone, and pregelatinised starch (maize)
1-855-274-4122 (Monday – Friday 8:30 AM to 5:00 PM EST) You may also report side effects to this phone number.
DISTRIBUTED BY:RITE AID,
30 HUNTER LANE, CAMP HILL,
PA 17011 www.riteaid.com
MADE IN INDIA
Code: AP/DRUGS/04/2016
Compare to the active Ingredient in Maximum Strength Mucinex®*
NDC 11822-4260-1
MAXIMUM STRENGTH
MUCUS
RELIEF
GUAIFENESIN EXTENDED-RELEASE
TABLETS 1200 mg
EXPECTORANT
Relieves chest congestion
Thins & loosens mucus
12
HOUR ACTUAL SIZE
14
EXTENDED-RELEASE
TABLETS
* Please review the disclaimer below.