Label: VICKS ZZZQUIL SOOTHING SLEEP NIGHTTIME SLEEP-AID- diphenhydramine hcl liquid

  • NDC Code(s): 69423-830-12, 69423-830-24
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each 30 mL)

    Diphenhydramine HCl 50 mg

  • Purpose

    Nighttime sleep-aid

  • Uses

    • for the relief of occasional sleeplessness
    • reduces time to fall asleep if you have difficulty falling asleep
  • Warnings

    Do not use

    • for children under 12 years of age
    • with any other product containing diphenhydramine, even one used on skin
  • Ask a doctor before use if you have

    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma
    • difficulty in urination due to enlargement of the prostate gland
    • a sodium-restricted diet
  • Ask a doctor or pharmacist before use if you are

    • taking sedatives or tranquilizers
  • When using this product

    • avoid alcoholic beverages
  • Stop use and ask a doctor if

    • sleeplessness persists continuously for more than 2 weeks. Insomnia may be a symptom of serious underlying medical illness.
  • 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 one dose (30 mL) per day (24 hours)
    • only use the dose cup provided

    adults & children 12 yrs & over30 mL at bedtime
    children under 12 yrsdo not use

  • Other information

    • each 30 mL dose contains: sodium 152 mg
    • store at no greater than 25°C
  • Inactive ingredients

    anhydrous citric acid, D&C Yellow No. 10, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavors (with chamomile and honey), glycerin, polysorbate 20, propylene glycol, saccharin sodium, sodium benzoate, sodium chloride, sodium citrate, sorbitol, sucralose, water

  • Questions?

    1-877-881-5813

  • SPL UNCLASSIFIED SECTION

    TAMPER EVIDENT: DO NOT USE IF PRINTED SHRINKBAND ON BOTTLE IS BROKEN OR MISSING.

  • SPL UNCLASSIFIED SECTION

    DIST. BY PROCTER & GAMBLE,

    CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 354 ml Bottle Label

    VICKS ®

    ZzzQuil™

    SOOTHING SLEEP

    NIGHTTIME SLEEP-AID

    Diphenhydramine HCl

    Fall Asleep Fast

    Wake Up Refreshed


    Chamomile Honey Flavored

    Non-Habit Forming

    Not for colds or for pain

    12 FL OZ (354 ml)

    830

  • INGREDIENTS AND APPEARANCE
    VICKS ZZZQUIL  SOOTHING SLEEP NIGHTTIME SLEEP-AID
    diphenhydramine hcl liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-830
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    HONEY (UNII: Y9H1V576FH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    CHAMOMILE (UNII: FGL3685T2X)  
    Product Characteristics
    ColoryellowScore    
    ShapeSize
    FlavorHONEY (Chamomile Honey) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-830-12354 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/06/2024
    2NDC:69423-830-242 in 1 CARTON02/06/2024
    2354 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 DrugM01002/06/2024
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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