Label: UP AND UP NIGHTTIME SLEEP-AID- diphenhydramine hydrochloride liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 16, 2015

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each 30 mL dose cup or 2 tablespoons)

    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
    •
    with other drugs that cause drowsiness such as antihistamines and nighttime cold/flu products

    Ask a doctor before use if you have

    •
    a breathing problem such as asthma, emphysema, or chronic bronchitis
    •
    glaucoma
    •
    difficulty in urination due to enlargement of the prostate gland
    •
    heart disease

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers or any other sleep aid

    When using this product

    •
    avoid alcoholic beverages and other drugs that cause drowsiness
    •
    drowsiness will occur
    •
    be careful when driving a motor vehicle or operating machinery

    Stop use and ask a doctor if sleeplessness persists continuously for more than two 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.

    Overdose warning

    Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    •
    take only one dose per day (24 hours) – see Overdose warning
    •
    use dose cup or tablespoon

    adults & children 12 yrs & over

    One Dose = 30 mL (2 tablespoons) at bed time if needed or as directed by a doctor
  • Other information

    •
    each 30 mL dose (2 tablespoons) contains: sodium 23 mg
    •
    store at room temperature
    •
    protect from light. Does not meet USP <671>.
  • Inactive ingredients

    anhydrous citric acid, FD&C blue 1, FD&C red 40, flavor, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum.

  • SPL UNCLASSIFIED SECTION

  • PRINCIPAL DISPLAY PANEL

    NDC 11673-730-92

    Compare to active ingredient in ZzzQuil™*


    nighttime

    sleep-aid

    diphenhydramine HCl

     
    non-habit forming
     
    alcohol free

    BERRY FLAVOR


    SEE WARNINGS NOT FOR TREATING COLD OR FLU

    12 FL OZ (354 mL)

    Failure to follow these warnings could result in serious consequences.

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

    *This product is not manufactured or distributed by Procter & Gamble, the distributor of ZzzQuil®

    Questions? Call 1-800-910-6874

    094 01 0778 R00 ID274446

    Distributed by Target Corporation Minneapolis, MN 55403

    ©2014 Target Brands, Inc.

    Shop Target.com

    up and up nighttime sleep aid Berry Flavor
  • INGREDIENTS AND APPEARANCE
    UP AND UP NIGHTTIME SLEEP-AID 
    diphenhydramine hydrochloride liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-730
    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
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Product Characteristics
    ColorPURPLEScore    
    ShapeSize
    FlavorBERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-730-92354 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 finalpart34110/20/2015
    Labeler - Target Corporation (006961700)
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