Active Ingredient
(in each extended-release tablet)
Guaifenesin USP 600 mg
The following Structured Product Label (SPL) was submitted to the FDA by Better Living Brands Llc for the product Guaifenesin (NDC 21130-179). 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 600 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 pregelatinized 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
BETTER LIVING BRANDS LLC
P.O.BOX 99, PLEASANTON, CA 94566-0009
1-888-723-3929
www.betterlivingbrandsLLC.com
MADE IN INDIA
CODE: AP/DRUGS/04/2016
Compare to
the active ingredient in
Mucinex®*
NDC 21130-179-67
Signature
Care®
Quality
Guaranteed
Mucus Relief
Guaifenesin Extended-Release
Tablets 600 mg
Expectorant
•Relieves Chest Congestion
•Thins And Loosens Mucus
12
HOUR
ACTUAL SIZE
20 EXTENDED-RELEASE TABLETS
* Please review the disclaimer below.