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Mucus Relief Sinus Severe Congestion Relief

Dosage form
TABLET, COATED
Labeler
DISCOUNT DRUG MART
Label updated
2024-10-17
Retrieved
2026-09-07
Active ingredients
ACETAMINOPHEN · GUAIFENESIN · PHENYLEPHRINE HYDROCHLORIDE
View original label and images on DailyMed ↗
Label information

Drug Facts

유효 성분

성분·작용

Active ingredients (in each caplet) Purpose
Acetaminophen 325 mg Pain reliever
Guaifenesin 200 mg Expectorant
Phenylephrine HCl 5 mg Nasal decongestant

Uses
  • temporarily relieves:
    • nasal congestion
    • headache
    • minor aches and pains
    • sinus congestion and pressure
  • promotes nasal and/or sinus drainage
  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
Warnings

Liver warning

This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 12 caplets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

Do not use

  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
  • if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.

Ask a doctor before use if you have

  • liver disease
  • heart disease
  • diabetes
  • high blood pressure
  • thyroid disease
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  • cough that occurs with too much phlegm (mucus)

Label information

Ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin

Label information

When using this product do not use more than directed

Stop use and ask a doctor if

  • nervousness, dizziness, or sleeplessness occur
  • pain, nasal congestion, or cough gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back or occurs with rash or persistent headache

These could be signs of a serious condition.

Label information

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

Label information

Keep out of reach of children.

Overdose warning

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions
  • do not take more than directed (see Overdose warning)
  • do not take more than 12 caplets in any 24-hour period
  • adults and children 12 years and older:  take 2 caplets every 4 hours
  • children under 12 years of age:  do not use
Other information
  • store between 20-25°C (68-77°F) in a dry place
  • retain outer package for complete product information
Inactive ingredients

colloidal silicon dioxide, croscarmellose sodium, crospovidone, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, povidone, pregelatinized starch, stearic acid, talc, titanium dioxide

PRINCIPAL DISPLAY PANEL

DISCOUNT drug mart FOOD FAIR

†Compare to the active ingredients in Mucinex® Sinus-Max™ Severe Congestion Relief

MAXIUMUM STRENGTH*

Mucus Relief

SINUS

Severe Congestion Relief

Acetaminophen, Guaifenesin, Phenylephrine HCl

Pain Reliever, Expectorant, Nasal Decongestant

• Clears Sinus Congestion

• Relieves Headache

• Thins & Loosens Mucus

For Ages 12+

20 CAPLETS

[Image in the official label — see DailyMed source]

DailyMed Set ID: f171a389-8b22-429c-86bc-272156fdc1b7 · Version 3
NDC: 53943-167