Label: MEIJER ADULT SEVERE MULTI-SYMPTOM COUGH COLD FLU- acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride liquid

  • NDC Code(s): 79481-6300-8
  • Packager: MEIJER DISTRIBUTION INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 1, 2026

If you are a consumer or patient please visit this version.

  • Active ingredients (in each 20 ml)

    Acetaminophen, USP 650 mg

    Dextromethorphan HBr, USP 20 mg

    Guaifenesin, USP 400 mg

    Phenylephrine HCl, USP 10 mg

  • Purposes

    Pain reliever/Fever reducer

    Cough suppressant

    Expectorant

    Nasal decongestant

  • INDICATIONS & USAGE

    Uses

    ▪
    temporarily relieves these symptoms occurring with a cold or flu:
    ▪
    cough due to minor throat and bronchial irritation
    ▪
    nasal congestion
    ▪
    sinus congestion and pressure
    ▪
    minor aches and pains
    ▪
    sore throat
    ▪
    headache
    ▪
    temporarily reduces fever
    ▪
    helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make coughs more productive
  • WARNINGS

    Warnings

    Liver warning

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

    ▪
    more than 6 doses in any 24-hour period, which is the maximum daily amount
    ▪
    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.

    Do not use

    ▪
    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.
    ▪
    with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

    Ask a doctor before use if you have

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

    Ask a doctor or pharmacist before use if you are

    ▪
    taking the blood thinning drug warfarin
    ▪
    taking any other oral nasal decongestant or stimulant
    ▪
    taking any other pain reliever/fever reducer

    When using this product do not use more than directed

    Stop use and ask a doctor if

    ▪
    you get nervous, dizzy, or sleepless
    ▪
    pain, cough, or nasal congestion 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 headache that lasts. These could be signs of a serious condition.

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

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Prompt medical attention is critical for adults as well as for children, even if you do not notice any signs or symptoms.

  • DOSAGE & ADMINISTRATION

    Directions

    ▪
    do not take more than 6 doses in any 24-hour period
    ▪
    do not exceed recommended dosage. Taking more than the recommended dose (overdose) may cause serious liver damage.
    ▪
    measure only with dosing cup provided
    ▪
    keep dosing cup with product
    ▪
    ml = milliliter
    ▪
    this adult product is not intended for use in children under 12 years of age
    agedose

    adults and children 12 years and over

    20 ml every 4 hours

    children under 12 years

    do not use

  • STORAGE AND HANDLING

    Other information

    •
    each 20 ml contains: sodium 7 mg
    •
    store at room temperature. Do not refrigerate.
  • INACTIVE INGREDIENT

    Inactive ingredients

    anhydrous citric acid, edetate disodium, FD&C red no. 40, glycerin, flavors, potassium citrate, propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol solution, sucralose, xanthan gum

  • QUESTIONS

    Questions or comments?

    1-866-467-2748

    Sugar-Free

    No Added Alcohol

  • SPL UNCLASSIFIED SECTION

    Distributed by:

  • PRINCIPAL DISPLAY PANEL

    Compare to the active ingredients in Adult Robitussin Maximum Strength SEVERE Multi-Symptom Cough Cold + Flu CF MAX*

    NDC 79481-6300-8

    MAXIMUM STRENGTH

    Adult

    SEVERE
    Multi-Symptom
    Cough Cold + Flu

    ACETAMINOPHEN (Pain Reliever/Fever Reducer)
    Dextromethorphan HBr (Cough Suppressant)
    Guaifenesin (Expectorant)
    Phenylephrine HCl (Nasal Decongestant)

    •
    Cough, Sore Throat
    •
    Body Aches, Fever
    •
    Nasal Congestion
    •
    Chest Congestion

    Natural Raspberry Flavor

    For Ages 12 & Over
    8 FL OZ (237 ml)

    *This product is not manufactured or distributed by GSK Consumer Healthcare, Owner of the registered trademark Adult Robitussin Maximum Strength SEVERE Multi-Symptom Cough Cold + Flu CF MAX.

    Meijer Adult SEVERE Multi Symptom Cough Cold + Flu 237 ml
  • INGREDIENTS AND APPEARANCE
    MEIJER ADULT SEVERE MULTI-SYMPTOM COUGH COLD FLU 
    acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79481-6300
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 20 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN400 mg  in 20 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorREDScore    
    ShapeSize
    FlavorRASPBERRY, CHOCOLATE, MINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79481-6300-81 in 1 CARTON03/31/2023
    1237 mL in 1 BOTTLE; Type 1: Convenience Kit of Co-Package
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/31/2023
    Labeler - MEIJER DISTRIBUTION INC (006959555)