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Pill Identifier Information of Diphenhydramine Hydrochloride 25 MG Oral Capsule

Drug Information

Diphenhydramine Hydrochloride 25 MG Oral Capsule

Imprint: PH014
Shape: C48336
Color: C48328
Ingredients: Diphenhydramine
Size: 14.00
Score: 1
Rxtty: SCD
Author: SDA Laboratories, Inc.
Inactive Ingredients: FERROSOFERRIC OXIDE / D&C RED NO. 28 / FD&C BLUE NO. 1 / FD&C RED NO. 40 / GELATIN / LACTOSE MONOHYDRATE / MAGNESIUM STEARATE / SILICON DIOXIDE / SODIUM LAURYL SULFATE >

Complete Information

  • Active ingredient (in each capsule)

    Diphenhydramine HCL 25 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

    • aAvoid 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 or over1 to 2 capsule                                     
    Children 6 to under 12 years1 capsule
    Children under 6 yearsask a doctor

  • 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

  • PRINCIPAL DISPLAY PANEL

    NDC 66424-020-10

    *Compare to active ingredient in BENADRYL® aLLERGY

    Diphenhydramine

    HCl Capsules, USP

    25 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 25 mg Capsule Package label

  • INGREDIENTS AND APPEARANCE
    DIPHENHYDRAMINE HCL 
    diphenhydramine hcl capsule
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66424-020
    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
    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 PH014
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66424-020-01100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/27/2010
    2NDC:66424-020-101000 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 DrugM01201/27/2010
    Labeler - SDA Laboratories, Inc. (948067889)
    Registrant - Pharbest Pharmaceuticals, Inc. (557054835)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharbest Pharmaceuticals, Inc.557054835manufacture(66424-020) , analysis(66424-020) , pack(66424-020) , label(66424-020)
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