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MUCUS RELIEF

Dosage form
TABLET
Labeler
Pioneer Life Sciences, LLC
Label updated
2025-07-04
Retrieved
2026-09-07
Active ingredients
GUAIFENESIN
View original label and images on DailyMed ↗
Active ingredient (in each tablet)

Guaifenesin 400 mg

Purpose

Expectorant

Uses
  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and makes 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 is accompanied by too much phlegm (mucus)
Stop use and ask a doctor if
  • cough lasts for more than 7 days, comes back, or occurs with fever, rash, or persistent headache. These could be signs of a serious illness.
Label information

If pregnant or breast-feeding,ask a health professional before use.

Label information

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions
  • Adults and children 12 years and older:take 1 tablet every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.
  • children under 12 years:do not use
Other information
  • Store at 25°C (77°F) excursions between 15°-30°C (59°-86°F)
  • Keep in a dry place and do not expose to heat
  • Read all product information before using
Inactive ingredients

Maltodextrin, Povidone, Microcrystalline cellulose, Croscarmellose sodium, Stearic acid, Magnesium sterate, Silicone dioxide.

Questions or Comments ?

Call +1 (732) 994-2808 or email [email protected]

Label information

This product is not manufcatured or distributed by Reckitt Benckiser's , owner of the Registered Trademark MUCINEX®

Label information

Distributed by: GenCare Consumer Products, LLC

40E Cotters Ln Suite A, East Brunswick, NJ 08816

포장 표시

[Image in the official label — see DailyMed source]

DailyMed Set ID: 8188b66a-5405-4e62-bde6-63ebc1f22b16 · Version 2
NDC: 72090-019