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Pill Identifier Information of Diphenhydramine Hydrochloride 25 MG Oral Tablet

Drug Information

Diphenhydramine Hydrochloride 25 MG Oral Tablet

Imprint: AZ;048
Shape: C48345
Color: C48328
Ingredients: Diphenhydramine
Size: 11.00
Score: 2
Rxtty: SCD
Author: Eagle Distributors,Inc.
Inactive Ingredients: croscarmellose sodium / D&C Red No. 27 / hypromelloses / lactose / magnesium stearate / cellulose, microcrystalline / polyethylene glycols / silicon dioxide / titanium dioxide>

Complete Information

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (in each caplet)

    Diphenhydramine HCl 25 mg

  • Purpose

    Antihistamine

  • Uses

    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

    • sneezing
    • runny nose
    • itchy, watery eyes
    • itching of the nose or throat
    • and these symptoms associated with the common cold:
      • sneezing
      • runny nose
  • Warnings

    Do not use with any other products containing diphenhydramine, including one used on skin

    Ask a doctor before use if you have
    • a breathing problem such as emphysema or chronic bronchitis
    • glaucoma or
    • 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 beverages
    • 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.

    Overdose warning

    In case of accidental overdose, contact a doctor or Poison Control Center immediately.

  • Directions

    • take every 4 to 6 hours
    • do not take more than 6 doses in 24 hours
    Adults and children 12 years of age and over1 to 2 caplets
    Children 6 to under 12 years1 caplet
    Children under 6 yearsConsult a doctor
  • Other information

  • Inactive ingredients

    croscarmellose sodium, D&C Red #27, hydroxypropylmethyl cellulose, lactose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, silicon dioxide, titanium dioxide. May contain polysorbate.

  • Questions or comments?

    Call toll free 1-800-570-8650 (M-F 9 am to 5 pm PST)

  • SPL UNCLASSIFIED SECTION

    *This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Benadryl®

    Product manufactured for:
    Eagle Distributors,Inc.
    Los Angeles, CA 90011

  • PRINCIPAL DISPLAY PANEL - 50 Pouch Carton

    Compare to the Active Ingredients in
    Bendaryl® Allergy*

    Allergy
    Get Relief

    Diphenhydramine Hci, An Antihistamine

    PRINCIPAL DISPLAY PANEL - 50 Pouch Carton
  • INGREDIENTS AND APPEARANCE
    ALLERGY GET RELIEF 
    diphenhydramine hydrochloride tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68737-223
    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)  
    hypromelloses (UNII: 3NXW29V3WO)  
    lactose (UNII: J2B2A4N98G)  
    magnesium stearate (UNII: 70097M6I30)  
    cellulose, microcrystalline (UNII: OP1R32D61U)  
    polyethylene glycols (UNII: 3WJQ0SDW1A)  
    silicon dioxide (UNII: ETJ7Z6XBU4)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorPINKScore2 pieces
    ShapeOVAL (Capsule shape) Size11mm
    FlavorImprint Code AZ;048
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68737-223-0750 in 1 BOX
    12 in 1 POUCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34106/30/2012
    Labeler - Eagle Distributors,Inc. (929837425)