Cold And Flu
FDA Label NDC 11673-779

Acetaminophen 650 mg
Dextromethorphan HBr 20 mg
Guaifenesin 400 mg
Phenylephrine HCl 10 mg 

Pain reliever/fever reducer
Cough suppressant
Expectorant
Nasal decongestant

Pain reliever/fever reducer
Cough suppressant
Nasal decongestant
Antihistamine

Acetaminophen 650 mg
Dextromethorphan HBr 20 mg
Phenylephrine HCl 10 mg
Triprolidine HCl 2.5 mg

• temporarily relieves these common cold and flu symptoms:
  
  • sore throat
    
  • nasal congestion
    
  • stuffy nose (Daytime only)
    
  • minor aches and pains
    
  • sneezing (Nighttime only)
    
  • headache
    
  • cough
    
  • runny nose (Nighttime only)
    
  • itching of the nose or throat (Nighttime only)
    
  • itchy, watery eyes due to hay fever (Nighttime only)
    
  • sinus congestion and pressure
    
  • temporarily reduces fever
    
  • controls cough to help you get to sleep (Nighttime only)
    
  • helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive (Daytime only)

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

• more than 4,000 mg of acetaminophen in 24 hours
• with other drugs containing acetaminophen
• 3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

• skin reddening
• blisters
• rash

If a skin reaction occurs, stop use and seek medical help right away.

Sore throat warning: If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

• 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.
  
• if you have ever had an allergic reaction to this product or any of its ingredients
  

• liver disease
• diabetes
• thyroid disease
  
• heart disease
• glaucoma (Nighttime only)
  
• difficulty in urination due to enlargement of the prostate gland
  
• cough that occurs with too much phlegm (mucus)
  
• persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema
  
• a breathing problem such as emphysema or chronic bronchitis (Nighttime only)
• high blood pressure
  

• taking the blood thinning drug warfarin
  
• taking sedatives or tranquilizers (Nighttime only)
  

• do not exceed recommended dosage
  
• excitability may occur, especially in children (Nighttime only)
  
• marked drowsiness may occur (Nighttime only)
  
• alcohol, sedatives, and tranquilizers may increase drowsiness (Nighttime only)
  
• avoid alcoholic beverages (Nighttime only)
  
• use caution when driving a motor vehicle or operating machinery (Nighttime only)
  

• nervousness, dizziness, or sleeplessness occur
  
• pain, nasal congestion, or cough gets worse or lasts more than 7 days
• new symptoms occur
  
• fever gets worse or lasts more than 3 days
  
• redness or swelling is present
  
• cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.
  

ask a health professional before use.

In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Do not take DAYTIME and NIGHTTIME products at the same time.

• do not take more than directed
  
• do not take more than 6 doses in any 24-hour period
  
• mL = milliliter; FL OZ = fluid ounce
  
• only use the dose cup provided
  
• adults and children 12 years and over: 20 mL in dosing cup provided every 4 hours
  
• children under 12 years: do not use
  

• do not take more than directed
  
• do not take more than 4 doses in any 24-hour period
  
• mL = milliliter; FL OZ = fluid ounce
  
• only use the dose cup provided
  
• adults and children 12 years and over: 20 mL in dosing cup provided every 4 hours
  
• children under 12 years: do not use
  

• each 20 mL contains: sodium 10 mg (Daytime only)
  
• store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
• use by expiration date on package
  

anhydrous citric acid, disodium edetate, FD&C blue #1, FD&C red #40, flavors, glycerin, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate dihydrate, sodium metabisulfite, sorbitol, sucralose, xanthan gum

anhydrous citric acid, FD&C blue #1, FD&C red #40, FD&C yellow #6, flavors, glycerin, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Call 1-800-910-6874

TOTAL 12 FL OZ (355 mL) - 2 x 6 FL OZ (177 mL) EACH

TAMPER EVIDENT: DO NOT
USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS
BROKEN OR MISSING

PARENTS:
Learn about teen medicine abuse
www.StopMedicineAbuse.org

094 14 0185 R00 C-001744-01-067
Distributed by Target Corporation
Minneapolis, MN 55403
TM & ©2022 Target Brands, Inc.

*This product is not manufactured or distributed by RB Health (US)
LLC, owner of the registered trademark Maximum Strength
Mucinex® Fast-Max® Cold & Flu and Maximum Strength Mucinex®
Nightshift® Severe Cold & Flu. 50844 ORG032204207845

Target 042078 (Target 44 042078 1)