Label: UP AND UP MUCUS RELIEF- guaifenesin tablet, extended release
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Contains inactivated NDC Code(s)
NDC Code(s): 11673-325-30, 11673-325-66 - Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 7, 2019
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- Official Label (Printer Friendly)
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Active ingredient (in each extended-release tablet)Guaifenesin 1200 mg
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PurposeExpectorant
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Useshelps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
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WarningsDo not use - • for children under 12 years of age - Ask a doctor before use if you have - • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or ...
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Directions• do not crush, chew, or break 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 and over: 1 ...
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Other information• store between 20°-25°C (68°-77°F) • do not use if printed foil under cap is broken or missing
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Inactive ingredientscolloidal silicon dioxide, copovidone, FD&C blue #1 aluminum lake, hypromellose, magnesium stearate, maltodextrin, microcrystalline cellulose, povidone, sodium starch glycolate Type A, stearic ...
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Questions or comments?1-888-547-7400
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Package/Label Principal Display PanelCompare to active ingredient in Maximum Strength Mucinex® maximum strength - mucus relief - guaifenesin extended-release tablets, 1200 mg - expectorant - relieves chest congestion - thins land loosens ...
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INGREDIENTS AND APPEARANCEProduct Information
