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DaytimeMulti-Symptom Cold/Flu Relief

Dosage form
CAPSULE, LIQUID FILLED
Labeler
Greenbrier International
Label updated
2012-07-28
Retrieved
2026-09-07
Active ingredients
ACETAMINOPHEN · Dextromethorphan Hydrobromide · Phenylephrine Hydrochloride
View original label and images on DailyMed ↗
Label information

Drug Facts

Active ingredients

Label information

Active ingredients (in each softgel)

Acetaminophen 325 mg

Dextromethorphan HBr 10 mg

Phenylephrine HCl 5 mg

Label information

 

Purpose

Label information

Purpose

Pain reliever/fever reducer

Cough suppressant

Nasal decongestant

Label information

 

Uses

temporarily relieves common cold/flu symptoms:

  • nasal congestion
  • cough due to minor throat & bronchial irritation
  • sore throat
  • headache
  • minor aches & pains
  • fever
Warnings

Liver warning

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

  • more than 4 doses in 24 hrs, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

Sore throat warning

If sore throat is severe, lasts for more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

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

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

  • you get nervous, dizzy or sleepless
  • symptoms get worse or last more than 5 days (children) or 7 days (adults)
  • 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 headache that lasts. 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 directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults & for children even if you do not notice any signs or symptoms.

Directions
  • take only as directed - see Overdose Warning
  • do not exceed 4 doses per 24 hrs
adults & children 12 yrs & over 2 LiquiCaps with water every 4 hrs
children 4 to under 12 yrs ask a doctor
children under 4 yrs do not use
Other information
  • store at room temperature
Inactive ingredients

FD&C Red No. 40, FD&C Yellow No. 6, gelatin, glycerin, methyl paraben, polyethylene glycol, povidone, propylene glycol, propyl paraben, purified water, sorbitol, titanium dioxide

Questions?

1-866-467-2748

Label information


Distributed by:

Greenbrier International, Inc.

Chesapeake, VA 23320

PRINCIPAL DISPLAY PANEL - 10 Softgel Carton

Multi-Symptom

 DayTime

Liquid Capsules

Acetaminophen, Dextromethorphan hydrobromide, Phenylephrine HCl

 

Cold/Flu Relief

  • Pain Reliever
  • Fever Reducer
  • Nasal Decongestant
  • Cough Suppressant

 

10 Softgels

Compare to the active ingredient in Vicks Dayquil®

[Image in the official label — see DailyMed source]

DailyMed Set ID: 6cf1fd3d-5529-412d-9003-a06edd445f57 · Version 1
NDC: 33992-0611