Label: MUCUS RELIEF- guaifenesin tablet, extended release
- NDC Code(s): 70000-0730-1
- Packager: LEADER/ Cardinal Health 110, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 16, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
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Active ingredient (in each extended-release tablet)
Guaifenesin, USP 1200 mg
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Purpose
Expectorant
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Uses
helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
- Warnings
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Do not use
for children under 12 years of age
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Ask a doctor before use if you have
persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough accompanied by too much phlegm (mucus)
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Stop use and ask a doctor if
cough lasts more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.
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If pregnant or breast-feeding,
ask a health professional before use.
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Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
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Directions
do not crush, chew, or break extended-release tablet - take with a full glass of water - this product can be administered without regard for the timing of meals - adults and children 12 years of age ...
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Other information
store at 20-25°C (68-77°F)
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Inactive ingredients
colloidal silicon dioxide, copovidone, FD&C blue no. 1 aluminum lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone (K-30), sodium starch glycolate, stearic ...
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Questions or comments?
Call - 1-877-290-4008
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PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information