Label: ALLERGY- diphenhydramine hcl tablet tablet

  • NDC Code(s): 66715-9711-7
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 15, 2023

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  • Drug Facts

  • Active Ingredient

    Active ingredient (in each tablet)
    Diphenhydramine HCl 25 mg

  • Purpose

    Anrihistamine

  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itching of the nose or throat
    • temporarily relieves these symptoms due to the common cold
    • runny nose
    • sneezing
  • Warnings

    ​Warnings

    Do not use

    • to make a child sleepy
    • 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
    • trouble urinating due to an enlarged prostate gland

    Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers.

    When using this product

    • marked drowsiness may occur
    • avoid alcoholic drinks
    • alcohol, sedatives and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children

    If pregnant or breast-feeding, ask a health professional before use.

    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).

  • Directions

    • take every 4 to 6 hours, or as directed by a doctor
    • do not take more than 6 doses in 24 hours
    • adults and children 12 years and over take 1 to 2 tablets
    • children 6 to under 12 years take 1 tablet
    • children under 6 years do not use
  • Other information

    • each tablet may contain: calcium 25mg
    • store at room temperature 68º-77ºF (20º-25ºC)
    • protect from light and moisture
  • Inactive ingredients

    croscarmellose sodium, D&C red #27 aluminum lake, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide

  • Questions or comments?

    call toll-free 1-877-507-6516 (M-F 8AM – 4:30PM CST)

  • Allergy (Lil' Drug Store) Pouch & Sleeve Label - PDP/Package

    [caduceus]

    Compare to the active ingredient in

    Benadryl ® Allergy ULTRATAB Tablets*

    Allergy

    Diphenhydramine HCl 25 mg

    Antihistamine

    Relieves

    • Runny Nose • Sneezing

    • Itchy, Watery Eyes

    • Itchy Nose or Throat

    *This product is not manufactured or distributed by

    Kenvue, Inc. Lil' Drug Store Products does not own the

    Benadryl Allergy ULTRATAB ® trademark.

    50 PACKETS OF 2 CAPLETS

    [UPC]

    3 66715 97117 3

    Pouch

    Label

  • INGREDIENTS AND APPEARANCE
    ALLERGY 
    diphenhydramine hcl tablet tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9711
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg
    Inactive Ingredients
    Ingredient NameStrength
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeCAPSULESize12mm
    FlavorImprint Code AZ048
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-9711-750 in 1 BOX, UNIT-DOSE09/12/2014
    12 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01209/12/2014
    Labeler - Lil' Drug Store Products, Inc. (093103646)
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