Label: NIGHTTIME CHILDRENS MULTI SYMPTOMS COLD AND COUGH MULTI-SYMPTOM RELIEF- chlorpheniramine maleate and dextromethorphan hydrobromide solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredients
    (in each 15 mL)
    Purpose

    Chlorpheniramine maleate 2 mg

    Antihistamine

    Dextromethorphan HBr 15 mg

    Cough suppressant

  • Uses

    temporarily relieves cold symptoms:

    cough due to minor throat & bronchial irritation
    sneezing
    runny nose
  • Warnings

    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.
    to make a child sleep

    Ask a doctor before use if you have

    glaucoma
    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
    trouble urinating due to enlarged prostate gland

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers.

    When using this product

    excitability may occur, especially in children
    marked drowsiness may occur
    avoid alcoholic drinks
    be careful when driving a motor vehicle or operating machinery
    alcohol, sedatives, & tranquilizers may increase drowsiness

    Stop use and ask a doctor if

    cough persists more than 1 week, tends to recur 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 at 1-800-222-1222.

  • Directions

    take only as directed
    do not exceed 4 doses per 24 hrs.
    only use the dose cup provided

    adults & children 12 yrs & over

    30 mL every 6 hrs.

    children 6 to under 12 yrs

    15 mL every 6 hrs.

    children 4 to under 6 yrs

    do not use unless directed by a doctor

    children under 4 yrs

    do not use

  • Other information

    each 15 mL contains: potassium 5 mg, sodium 5 mg
    store at room temperature
  • Inactive ingredients

    anhydrous citric acid, FD&C Red No. 40, flavor, potassium citrate, potassium sorbate, propylene glycol, purified water, sodium benzoate, sorbitol, sucrose

  • Questions or comments?

    1-888-287-1915

  • PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

    Compare to Children’s Vicks Nyquil™ active ingredients*

    equate™

    NDC 49035-545-08

    Childrens

    Sugar-Free

    Multi-Symptoms
    Cold & Cough

    NIGHTTIME

    Chlorpheniramine maleate 2 mg,

    Dextromethorphan HBr 15 mg

    Sneezing
    Runny Nose
    Cough

    Aspirin-Free

    Acetaminophen-Free

    Natural Cherry Flavor

    Free of Alcohol & Acetaminophen

    8 FL OZ (236 ml)

    DISTRIBUTED BY: Walmart Inc.,

    Bentonville, AR 72716

    Made in the USA

    With domestic and imported ingredients Factory Certified

    TAMPER EVIDENT: Do not use if printed shrink band is missing or broken.

    *This product is manufactured or distributed by Procter & Gamble, the distributor of Children’s Vicks® Nyquil™

    Satisfaction guaranteed – Or we’ll replace it or give you your money back. For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915

    Walmart Nighttime Children's Multi Symptom cold and cough
  • INGREDIENTS AND APPEARANCE
    NIGHTTIME CHILDRENS MULTI SYMPTOMS  COLD AND COUGH MULTI-SYMPTOM RELIEF
    chlorpheniramine maleate and dextromethorphan hydrobromide solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49035-545
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE2 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE15 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorREDScore    
    ShapeSize
    FlavorCHERRY (Natural Cherry Flavor) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49035-545-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/30/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/30/2020
    Labeler - WAL-MART STORES,INC. (051957769)