Label: GOOD SENSE SLEEP TIME- diphenhydramine hcl solution

  • NDC Code(s): 0113-0186-30, 0113-0186-40
  • Packager: L. Perrigo Company
  • 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 September 18, 2017

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

  • Active ingredient (in each 30 mL)

    Diphenhydramine HCl 50 mg

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  • Purpose

    Nighttime sleep-aid

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  • Uses

    for the relief of occasional sleeplessness
    reduces time to fall asleep if you have difficulty falling asleep
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  • 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 an enlargement of the prostate gland

    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.

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  • Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

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  • Directions

    take only one dose per day (24 hours)
    only use the dose cup provided

    adults & children 12 yrs & over

    30 mL at bed time if needed or as directed by a doctor

    children under 12 yrs

    do not use

    Other information

    each 30 mL contains: sodium 20 mg
    store at 20-25˚C (68-77˚F)
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  • Inactive ingredients

    alcohol, anhydrous citric acid, FD&C blue #1, FD&C red #40, flavor, high fructose corn syrup, poloxamer 407, propylene glycol, purified water, saccharin sodium, sodium benzoate, sodium citrate

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  • Questions or comments?

    1-800-719-9260

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  • Package/Label Principal Display Panel

    Non-Habit Forming

    SleepTime

    Nighttime Sleep-Aid

    Diphenhydramine HCl

    50 mg per 30 mL

    Berry Flavor

    Not For Treating Cold or Flu

    Compare to active ingredient of Vicks® ZzzQuil®

    100% SATISFACTION GUARANTEED

    6 FL OZ (177 mL)

    ALCOHOL 10%

    186-c2-sleeptime-1.jpg
    186-c2-sleeptime-2.jpg
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  • INGREDIENTS AND APPEARANCE
    GOOD SENSE SLEEP TIME 
    diphenhydramine hcl solution
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0186
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE 50 mg  in 30 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Product Characteristics
    Color PURPLE Score     
    Shape Size
    Flavor BERRY Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0113-0186-30 177 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/02/2013
    2 NDC:0113-0186-40 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/02/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part338 07/02/2013
    Labeler - L. Perrigo Company (006013346)
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