Label: VICKS DAYQUIL KIDS HONEY AND VICKS NYQUIL KIDS HONEY COLD AND COUGH PLUS- doxylamine succinate, phenylephrine hydrochloride, dextromethorphan hydrobromide kit

  • NDC Code(s): 69423-946-08, 69423-983-08, 69423-993-16
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 16, 2023

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  • SPL UNCLASSIFIED SECTION

    NyQuil Kids HONEY COLD & COUGH + CONGESTION

    Drug Facts

  • Active ingredients (in each 15 mL)

    Dextromethorphan HBr 10 mg
    Doxylamine succinate 6.25 mg
    Phenylephrine HCl 5 mg

  • Purpose

    Cough suppressant
    Antihistamine
    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 • runny nose & sneezing
    • reduces swelling of nasal passages
    • temporarily restores freer breathing through the nose
    • promotes nasal and/or sinus drainage

  • 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 sleepy

  • Ask a doctor before use if you have

    • heart disease

    • high blood pressure
    • thyroid disease

    • diabetes

    • glaucoma
    • trouble urinating due to enlarged prostate gland
    • cough that occurs with too much phlegm (mucus)
    • a breathing problem or chronic cough that lasts or occurs with smoking, asthma 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.
    • excitability may occur, especially in children
    • marked drowsiness may occur
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • avoid alcoholic drinks
    • be careful when driving a motor vehicle or operating machinery

  • 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

    Keep out of reach of children.

  • In case of overdose,

    get medical help or contact a Poison Control Center right away.

  • Directions

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

    adults & children 12 yrs & over30 mL every 4 hrs
    children 6 to under 12 yrs15 mL every 4 hrs
    children 4 to under 6 yrsdo not use unless directed by a doctor
    children under 4 yrsdo not use


  • Other information

    • each 15 mL contains: sodium 14 mg
    • store at no greater than 25°C
  • Inactive ingredients

    citric acid, D&C Yellow No. 10, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavor (with honey), glycerin, propylene glycol, saccharin sodium, sodium benzoate, sodium citrate, sorbitol, sucralose, water, xanthan gum

  • Questions?

    1-800-362-1683

  • SPL UNCLASSIFIED SECTION

    DayQuil Kids HONEY COLD & COUGH + MUCUS

    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

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

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

    adults & children 12 yrs & over30 mL every 4 hrs
    children 6 to under 12 yrs15 mL every 4 hrs
    children 4 to under 6 yrsask a doctor
    children under 4 yrsdo not use
  • Other information

    • each 15 mL contains: sodium 14 mg
    • store at no greater than 25°C
  • Inactive ingredients

    citric acid, D&C Yellow No. 10, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavor (with honey), glycerin, propylene glycol, saccharin sodium, sodium benzoate, sodium citrate, sorbitol, sucralose, water, xanthan gum

  • Questions?

    1-800-362-1683

  • SPL UNCLASSIFIED SECTION

    TAMPER EVIDENT: Do not use if printed shrinkband seal around the neck is broken or missing.

  • PRINCIPAL DISPLAY PANEL - Convenience Pack

    VALUE COMBO PACK

    1 DAY + 1 NIGHT

    VICKS ®

    DayQuil ™ Kids HONEY

    COLD & COUGH + MUCUS

    Guaifenesin, Phenylephrine HCl, Dextromethorphan HBr

    Chest Congestion
    Nasal Congestion
    Cough

    Non-Drowsy

    FREE OF ALCOHOL
    & ACETAMINOPHEN

    NyQuil ™ Kids HONEY

    COLD & COUGH + CONGESTION

    Doxylamine Succinate, Phenylephrine HCl, Dextromethorphan HBr

    Sneezing, Runny Nose
    Nasal Congestion
    Cough

    ​ Nighttime Relief

    2 BOTTLES - 1 DAYQUIL/1 NYQUIL 8 FL OZ (236 mL) EACH; TOTAL 16 FL OZ (473 mL)

    993

  • INGREDIENTS AND APPEARANCE
    VICKS DAYQUIL KIDS HONEY AND VICKS NYQUIL KIDS HONEY  COLD AND COUGH PLUS
    doxylamine succinate, phenylephrine hydrochloride, dextromethorphan hydrobromide kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-993
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-993-161 in 1 PACKAGE; Type 0: Not a Combination Product07/12/2022
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BOTTLE, PLASTIC 236 mL
    Part 21 BOTTLE, PLASTIC 236 mL
    Part 1 of 2
    VICKS DAYQUIL KIDS  COLD COUGH PLUS MUCUS
    guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid
    Product Information
    Item Code (Source)NDC:69423-946
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN100 mg  in 15 mL
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-946-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/08/2021
    Part 2 of 2
    VICKS NYQUIL KIDS  HONEY COLD COUGH CONGESTION
    doxylamine succinate, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid
    Product Information
    Item Code (Source)NDC:69423-983
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE5 mg  in 15 mL
    DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE10 mg  in 15 mL
    DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE6.25 mg  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorHONEYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-983-08236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/07/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01207/12/2021
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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