Active Ingredient(S)
Guaifenesin USP, 600 mg (for 600mg)
Guaifenesin USP, 1200 mg (for 1200 mg)
The following Structured Product Label (SPL) was submitted to the FDA by Strategic Sourcing Services, Llc for the product Guaifenesin 600 Mg (NDC 70677-1257). 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(s), purpose, use(s), warnings, do not use, ask a doctor before use if, stop use and ask doctor if, if pregnant or breastfeeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Guaifenesin USP, 600 mg (for 600mg)
Guaifenesin USP, 1200 mg (for 1200 mg)
Expectorant
persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
cough accompanied by too much phlegm (mucus)
ask a health professional before use.
In case of overdose, get medical help or contact aPoison Control Center right away (1-800-222-1222).
carbomer homopolymer type B, colloidal silicon dioxide, ferric oxide red, hydroxypropyl cellulose, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate type A
call 1-833-358-6431 Monday to Friday 9:00am to 7:00pm EST
You may also report side effects to this phone number.
Guaifenesin Extended-Release Tablets 600 mg
Carton Label
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