Label: WALGREEN DAYTIMEL KIDS COLD COUGH PLUS MUCUS- guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid

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

Drug Label Information

Updated November 12, 2024

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients (in each 15 mL)

    Dextromethorphan HBr 10 mg
    Guaifenesin 100 mg

    Phenylephrine HCl 5 mg

    Purpose

    Cough suppressant
    Expectorant

    Nasal decongestant

  • Uses

    temporarily relieves common cold symptoms:
    nasal congestion
    sinus congestion & pressure
    cough due to minor throat & bronchial irritation
    cough to help you sleep
    reduces swelling of nasal passages
    temporarily restores freer breathing through the nose
    promotes nasal and/or sinus drainage
    helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive..
  • 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.

    Ask a doctor before use if you have

    heart disease
    high blood pressure
    thyroid disease
    diabetes
    trouble urinating due to enlarged prostate gland
    cough that occurs with too much phlegm (mucus)
    persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema

    When using this product, do not use more than directed.

    Stop use and ask a doctor if

    you get nervous, dizzy or sleepless
    symptoms do not improve within 7 days or occur with a fever
    cough persists for more than 7 days, comes back or occurs with a 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.

    Overdose warning

    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
    use dose cup provided
    do not exceed 4 doses per 24 hrs


    adults & children 12 yrs & over 30 mL every 4 hrs

    children 6 to under 12 yrs 15 mL every 4 hrs

    children 4 to under 6 yrs ask a doctor

    children under 4 yrs do not use

  • Other information

    each 15 mL contains: sodium 12 mg
    store at room temperature
  • Inactive ingredients

    citric acid, carboxymethyl cellulose sodium, D&C Yellow No. 10, disodium edetate, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

  • Questions?

    1-866-467-2748

  • SPL UNCLASSIFIED SECTION

    Distributed by:

  • PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

    Compare to the active ingredients in Kids Vicks ® DayQuil™ Honey Cold & Cough + Mucus

    NDC 0363-6238-08

    Daytime

    Kid’s

    Cold & Cough + Mucus

    Guaifenesin, Phenylephrine HCl, Dextromethorphan HBr

    Chest Congestion
    Nasal Congestion
    Cough

    No Added Alcohol & Acetaminophen free

    Honey Flavor

    Naturally and Artificially Flavored

    8 FL OZ (236 mL)

    *This product is not manufactured or distributed by Procter & Gamble, the distributor of Kids Vicks ® DayQuil™ Honey Cold & Cough + Mucus.

    WAG Daytime Kids Cold & cough + mucus Honey Flavor 8 FL OZ
  • INGREDIENTS AND APPEARANCE
    WALGREEN DAYTIMEL KIDS  COLD COUGH PLUS MUCUS
    guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-6238
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 15 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYL GALLATE (UNII: 8D4SNN7V92)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-6238-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/01/2023
    Labeler - WALGREENS CO. (008965063)