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← US medicinesUS · Over-the-counter medicine
mucus relief
- Dosage form
- TABLET, MULTILAYER, EXTENDED RELEASE
- Labeler
- Meijer Distribution Inc
- Label updated
- 2025-06-05
- Retrieved
- 2026-09-07
- Active ingredients
- GUAIFENESIN
Active ingredient (in each extended-release tablet)
Guaifenesin 600 mg
Purpose
Expectorant
Uses
-
• helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
Warnings
Do 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 emphysema -
• cough accompanied by too much phlegm (mucus)
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.
If pregnant or breast-feeding,
ask a health professional before use.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
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 or 2 tablets every 12 hours. Do not exceed 4 tablets in 24 hours. -
• children under 12 years of age: do not use
Other information
-
• store between 20-25°C (68-77°F)
Inactive ingredients
carbomer homopolymer type B, FD&C blue #1 aluminum lake, hypromellose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate
Questions or comments?
1-800-719-9260
Package/Label Principal Display Panel
meijer®
COMPARE TO MUCINEX® ACTIVE INGREDIENT
Mucus Relief
Guaifenesin Extended-Release Tablets, 600 mg/Expectorant
12 HOUR
RELIEVES CHEST CONGESTION
THINS AND LOOSENS MUCUS
IMMEDIATE AND EXTENDED RELEASE
40 EXTENDED-RELEASE TABLETS
Actual Size
[Image in the official label — see DailyMed source]
DailyMed Set ID: 68ae00cb-8e33-4bf5-9c86-c6356e70f8a4 · Version 5
NDC: 41250-684