Label: ROBITUSSIN HONEY SEVERE COUGH, FLU PLUS SORE THROAT- acetaminophen, dextromethorphan hbr solution

  • NDC Code(s): 0031-8771-12, 0031-8771-18
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 26, 2024

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  • Active ingredients (in each 20 mL)

    Acetaminophen, USP 650 mg

    Dextromethorphan HBr 20 mg

  • Purposes

    Pain reliever/Fever reducer

    Cough suppressant

  • INDICATIONS & USAGE

    Uses

    •
    temporarily relieves these symptoms occurring with a cold or flu:
    •
    cough due to minor throat and bronchial irritation
    •
    minor aches and pains
    •
    sore throat pain
    •
    headache
    •
    temporarily reduces fever
  • 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
    •
    cough that occurs with too much phlegm (mucus)
    •
    a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, or emphysema

    Ask a doctor or pharmacist before use if you are

    •
    taking the blood thinning drug warfarin
    •
    taking any other pain reliever/fever reducer

    When using this product do not use more than directed.

    Stop use and ask a doctor if

    •
    pain 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 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. 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 21 mg
    •
    store at 20-25°C (68-77°F). Do not refrigerate.
  • INACTIVE INGREDIENT

    Inactive ingredients

    anhydrous citric acid, carboxymethylcellulose sodium, glycerin, natural & artificial flavors, natural grade A honey, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium gluconate, sucralose, xanthan gum, zinc gluconate

  • QUESTIONS

    Questions or comments?

    call weekdays from 8 AM to 6 PM EST at 1-800-245-1040

  • Additional information

    Packaged with Tamper-Evident bottle cap. Do Not Use if breakable ring is separated or missing.

    PARENTS:

    Learn about teen medicine abuse

    www.StopMedicineAbuse.org

    Distributed by: Haleon, Warren, NJ 07059

    ©2024 Haleon group of companies or its licensor.

    Trademarks are owned by or licensed to the Haleon group of companies.

    For most recent product information, visit www.robitussin.com

    Pat. Info www.productpats.com

    Made in Canada

  • PRINCIPAL DISPLAY PANEL

    Robitussin

    Honey

    ADULT

    SEVERE
    Cough, Flu +
    Sore Throat

    ACETAMINOPHEN (Pain Reliever/Fever Reducer)
    DEXTROMETHORPHAN HBr (Cough Suppressant)

    NON-DROWSY

    MAXIMUM STRENGTH

    ✓
    Controls Cough
    ✓
    Soothes Sore Throat Pain
    ✓
    Relieves Fever & Body Aches

    Taste the Real Honey
    with Elderberry

    CF
    MAX

    For Ages 12+

    8 FL OZ (237 mL)

    62000000207916 – Front Carton

    Robitussin Honey CF Max 8 fl ozs
  • INGREDIENTS AND APPEARANCE
    ROBITUSSIN HONEY SEVERE COUGH, FLU PLUS SORE THROAT 
    acetaminophen, dextromethorphan hbr solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-8771
    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
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HONEY (UNII: Y9H1V576FH)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SODIUM GLUCONATE (UNII: R6Q3791S76)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ZINC GLUCONATE (UNII: U6WSN5SQ1Z)  
    Product Characteristics
    ColorORANGEScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0031-8771-121 in 1 CARTON06/15/2020
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:0031-8771-181 in 1 CARTON06/15/2020
    2237 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01206/15/2020
    Labeler - Haleon US Holdings LLC (079944263)
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