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Mucinex

Dosage form
TABLET, EXTENDED RELEASE
Labeler
State of Florida DOH Central Pharmacy
Label updated
2013-09-26
Retrieved
2026-09-07
Active ingredients
GUAIFENESIN
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredient (in each extended-release bi-layer 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

Label information

Do not use

  • for children under 12 years of age

Label information

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)

Label information

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.

Label information

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

Label information

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
Label information

Other information

  • store between 20-25°C (68-77°F)
  • see window for lot number and expiration date

Questions? 1-866-MUCINEX (1-866-682-4639)

You may also report side effects to this phone number

Please visit our web site www.mucinex.com

US Pat. 6,372,252 B1

US Pat. 6,955,821 B2

Inactive ingredients

carbomer homopolymer type B, FD&C blue #1 aluminum lake; hypromellose, USP; magnesium stearate, NF; microcrystalline cellulose, NF; sodium starch glycolate, NF

Keep Out of Reach of Children

Keep out of reach of children. This package is intended for institutional use only. This package is not child resistant. In case of overdose, get medical help or contact a Poison Control Center right away.

Label information

Dist. by:
Reckitt Benckiser Inc.
Parsippany, NJ 07054-0224

Repackaged by: Cardinal Health Zanesville, OH 43701

This Product was Repackaged By:

State of Florida DOH Central Pharmacy
104-2 Hamilton Park Drive
Tallahassee, FL 32304
United States

PACKAGE LABEL

Label Image for 53808-0871
600mg

[Image in the official label — see DailyMed source]

DailyMed Set ID: 594ad1e6-4221-4a4a-89db-a214ddf8306e · Version 1
NDC: 53808-0871