Label: DIPHENHYDRAMINE HCL capsule

  • NDC Code(s): 66424-021-01, 66424-021-10
  • Packager: SDA Laboratories, Inc.
  • 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 June 13, 2023

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  • Active ingredient (in each capsule)

    Diphenhydramine HCL 50 mg

    Purpose

    Antihistamine

  • Uses:

    Temporarily relieves these symptoms associated with the common cold, hay fever, or other respiratory allergies

    • sneezing
    • nasal congestion
    • runny nose
    • itchy, watery eyes
  • Warnings:

  • Do not use

    • With any other product containing Diphenhydramine HCL, including one applied topically.
  • Ask a doctor or pharmacist before use

    If you have

    • trouble urinating due to enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma
    • if you are taking sedatives or tranquilizers
  • When using this product

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

  • Directions:

    • Take every 4-6 hours
    • Do not take more than 6 doses in 24 hours.
    Adults and children 12 years & over1 capsule                                     
    Children under 12 yearsask a doctor

    **25 mg strength is not available in this package. Do not attempt to break capsules.

  • Other information:

    • Store at room temperature 15-30  degrees C (59-86 degrees F)
    • Protect from excessive moisture
  • Inactive ingredients: 

    Black Iron Oxide, D & C Red #28, FD & C Blue #1, FD & C Red #40, Gelatin, Lactose Monohydrate, Magnesium Stearate, Silicon Dioxide, Sodium Lauryl Sulfate

  • Questions? Adverse drug event call:

    1-800-687-0176

  • PRINCIPAL DISPLAY PANEL

    SDA Diphenhydramine HCl 50 mg Capsule Package labelNDC 66424-021-10

    *Compare to active ingredient in BENADRYL® ALLERGY

    Diphenhydramine

    HCl Capsules, USP

    50 mg

    TAMPER-EVIDENT: DO NOT USE IF IMPRINTED SAFETY

    SEAL UNDER CAP IS MISSING OR DAMAGED

    ANTIHISTAMINE

    1000 CAPSULES

    Not for house holds with young children

    SDA

    Laboratories, Inc.

    THIS PACKAGE FOR HOUSEHOLDS WITHOUT YOUNG CHILDREN

    SDA Diphenhydramine HCl 50 mg Capsule Package label

  • INGREDIENTS AND APPEARANCE
    DIPHENHYDRAMINE HCL 
    diphenhydramine hcl capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66424-021
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE50 mg
    Inactive Ingredients
    Ingredient NameStrength
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    D&C RED NO. 28 (UNII: 767IP0Y5NH)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    GELATIN (UNII: 2G86QN327L)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeCAPSULESize14mm
    FlavorImprint Code PH013
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66424-021-01100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/27/2010
    2NDC:66424-021-101000 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/27/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34101/27/2010
    Labeler - SDA Laboratories, Inc. (948067889)
    Registrant - Pharbest Pharmaceuticals, Inc. (557054835)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharbest Pharmaceuticals, Inc.557054835manufacture(66424-021) , analysis(66424-021) , pack(66424-021) , label(66424-021)
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