Active Ingredient
(in each extended-release tablet)
Guaifenesin USP 1200 mg
The following Structured Product Label (SPL) was submitted to the FDA by Innovus Pharmaceuticals, Inc. for the product Guaifenesin (NDC 57483-144). 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)
Distributed By: Innovus Pharmaceuticals, Inc.
5740 Kietzke Lane #300, Reno, Nevada 89511
www.crclehealth.com
Made in India
*Compare to the active
ingredient of Maximum
Strength Mucinex®
C•rcle™
NDC 57483-144-28
Maximum Strength
Guaifenesin
Extended-Release Tablets 1200 mg
Guaifenesin 1200 mg - Expectorant
RELIEVES CHEST CONGESTION
12
Hour
28 EXTENDED-RELEASE TABLETS
Actual Size
* Please review the disclaimer below.