Label: ROBITUSSIN DAY AND NIGHT COUGH RELIEF VALUE PACK- dextromethorphan hydrobromide, guaifenesin, chlorpheniramine maleate kit

  • NDC Code(s): 0031-2099-01, 0031-8692-13, 0031-8702-13
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 15, 2025

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  • Active ingredients (in each 20 mL)– Children’s Robitussin Cough & Chest Congestion DM

    Dextromethorphan HBr 20 mg

    Guaifenesin 200 mg

  • Purposes– Children’s Robitussin Cough & Chest Congestion DM

    Cough Suppressant

    Expectorant

  • Uses– Children’s Robitussin Cough & Chest Congestion DM

    • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
    • helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
  • Warnings– Children’s Robitussin Cough & Chest Congestion DM

    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.

    Ask a doctor before use if you have

    • cough that occurs with too much phlegm (mucus)
    • cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema

    Stop use and ask a doctor if

    cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.

    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.

  • Directions– Children’s Robitussin Cough & Chest Congestion DM

    • do not take more than 6 doses in any 24-hour period
    • measure only with dosing cup provided
    • keep dosing cup with product
    • mL = milliliter

    age

    dose

    children under 4 years

    do not use

    children 4 to under 6 years

    5 mL every 4 hours

    children 6 to under 12 years

    10 mL every 4 hours

    adults and children 12 years and over

    20 mL every 4 hours
  • Other information– Children’s Robitussin Cough & Chest Congestion DM

    • each 20 mL contains:sodium 21 mg
    • store at 20-25°C (68-77°F). Do not refrigerate.
  • Inactive ingredients– Children’s Robitussin Cough & Chest Congestion DM

    anhydrous citric acid, carboxymethylcellulose sodium, FD&C blue no. 1, FD&C red no. 40, glycerin, liquid glucose, natural and artificial flavors, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium gluconate, sucralose, xanthan gum

  • Questions or comments?– Children’s Robitussin Cough & Chest Congestion DM

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

  • Active ingredients (in each 10 mL)– Children’s Robitussin Nighttime Cough Long-Acting DM

    Chlorpheniramine maleate, USP 2 mg

    Dextromethorphan HBr, USP 15 mg

  • Purposes –Children’s Robitussin Nighttime Cough Long-Acting DM

    Antihistamine

    Cough suppressant

  • Uses –Children’s Robitussin Nighttime Cough Long-Acting DM

    • temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
      • runny nose
      • sneezing
      • itchy, watery eyes
      • itching of the nose or throat
  • Warnings– Children’s Robitussin Nighttime Cough Long-Acting DM

    Do not use

    • to sedate a child or to make a child sleepy
    • 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

    • trouble urinating due to an enlarged prostate gland
    • glaucoma
    • a 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 sedatives or tranquilizers.

    When using this product

    • do not use more than directed
    • marked drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children

    Stop use and ask a doctor if

    cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.

    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.

  • Directions –Children’s Robitussin Nighttime Cough Long-Acting DM

    • measure only with dosing cup provided
    • keep dosing cup with product
    • mL = milliliter
    • do not take more than 4 doses in any 24-hour period

    age

    dose

    children under 6 years

    do not use

    children 6 to under 12 years

    10 mL every 6 hours

    adults and children 12 years and over

    20 mL every 6 hours
  • Other information –Children’s Robitussin Nighttime Cough Long-Acting DM

    • each 10 mL contains:sodium 6 mg
    • store at 20-25°C (68-77°F)
  • Inactive ingredients –Children’s Robitussin Nighttime Cough Long-Acting DM

    anhydrous citric acid, FD&C red no. 40, glycerin, lactic acid, natural and artificial flavors, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose

  • Questions or comments? –Children’s Robitussin Nighttime Cough Long-Acting DM

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

  • Additional Information – Children’s Robitussin Day & Night Cough Relief Value Pack

    TAMPER-EVIDENT INNER UNITS:

    Do Not Use if Tamper-Evident feature on either bottle cap is broken or missing. See individual inner cartons and bottle labels for specific Tamper-Evident features.

    Do not take both products within 6 hours of each other.

    Children’s Robitussin liquid is specially formulated to provide soothing action, control your child’s cough – plus relieves other cold symptoms.

    PARENTS:Learn about teen medicine abuse

    www.StopMedicineAbuse.org

  • Principal Display Panel – Children’s Robitussin Day & Night Cough Relief Value Pack

    DAY & NIGHT

    COUGH RELIEF

    VALUE PACK

    Children’s Robitussin

    AGES 4 & OVER

    Cough & Chest Congestion DM

    DEXTROMETHORPHAN HBr

    (Cough Suppressant)

    GUAIFENESIN

    (Expectorant)

    Relieves:

    • Chest Congestion/Mucus
    • Cough

    grapeflavor

    4 FL OZ (118 mL)

    AGES 6 & OVER

    Nighttime Cough Long-Acting DM

    CHLORPHENIRAMINE MALEATE

    (Antihistamine)

    DEXTROMETHORPHAN HBr (Cough Suppressant)

    Relieves:

    • Cough Up to 8 Hours
    • Runny Nose

    Alcohol-free

    fruit punchflavor

    4 FL OZ (118 mL)

    Day Night Robitussin Childrens Cough Combo Kit
  • Principal Display Panel – Children’s Robitussin Cough & Chest Congestion DM

    Children’s

    Robitussin

    FOR AGES 4 & OVER

    Cough & Chest Congestion DM

    DEXTROMETHORPHAN HBr
    (Cough Suppressant)

    GUAIFENESIN
    (Expectorant)

    Relieves:

    • Chest Congestion/Mucus
    • Cough

    BETTER TASTING!*

    Great Grape Taste

    grapeflavor

    4 FL OZ (118 mL)

    Childrens Robitussin Cough Chest Congestion DM 4 FL OZ
  • Principal Display Panel – Children’s Robitussin Nighttim e Cough DM

    Children’s

    Robitussin

    AGES 6 & OVER

    Nighttime Cough DM

    Long-Acting

    CHLORPHENIRAMINE MALEATE
    (Antihistamine)

    DEXTROMETHORPHAN HBr
    (Cough Suppressant)

    Relieves:

    • Cough Up to 8 Hours
    • Runny Nose

    Alcohol-Free

    fruit punchflavor

    4 FL OZ (118 mL)

    Childrens Robitussin Nighttime Cough DM 4 FL OZ
  • INGREDIENTS AND APPEARANCE
    ROBITUSSIN   DAY AND NIGHT COUGH RELIEF VALUE PACK
    dextromethorphan hydrobromide, guaifenesin, chlorpheniramine maleate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0031-2099
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0031-2099-011 in 1 CARTON; Type 0: Not a Combination Product05/12/2020
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE 118 mL
    Part 21 BOTTLE 118 mL
    Part 1 of 2
    CHILDRENS ROBITUSSIN COUGH AND CHEST CONGESTION DM 
    dextromethorphan hydrobromide and guaifenesin liquid
    Product Information
    Item Code (Source)NDC:0031-8702
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN200 mg  in 20 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    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)  
    Product Characteristics
    ColorpurpleScore    
    ShapeSize
    FlavorGRAPEImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0031-8702-131 in 1 CARTON
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/12/2020
    Part 2 of 2
    CHILDRENS ROBITUSSIN NIGHTTIME COUGH LONG-ACTING DM 
    chlorpheniramine maleate, dextromethorphan hydrobromide solution
    Product Information
    Item Code (Source)NDC:0031-8692
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg  in 10 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorFRUIT PUNCHImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0031-8692-131 in 1 CARTON
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/12/2020
    Labeler - Haleon US Holdings LLC (079944263)
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