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Pill Identifier Information of Diphenhydramine Hydrochloride 25 MG Oral Tablet

Drug Information

Diphenhydramine Hydrochloride 25 MG Oral Tablet

Imprint: 44;329
Shape: C48337
Color: C48328
Ingredients: Diphenhydramine
Size: 11.00
Score: 1
Rxtty: SCD
Author: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Inactive Ingredients: CELLULOSE, MICROCRYSTALLINE / D&C RED NO. 27 / ANHYDROUS DIBASIC CALCIUM PHOSPHATE / MAGNESIUM STEARATE / POLYETHYLENE GLYCOL / POLYVINYL ALCOHOL / SILICON DIOXIDE / STEARIC ACID / TITANIUM DIOXIDE

Complete Information

  • Active ingredient (in each tablet)

    Diphenhydramine HCl 25 mg

  • Purpose

    Antihistamine

  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
      • runny nose
      • itchy, watery eyes
      • sneezing
      • itching of the nose or throat
  • temporarily relieves these symptoms due to the common cold:
    • runny nose
    • sneezing
  • 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
    • difficulty in urination due to enlargement of the prostate gland

    • Ask a doctor or pharmacist before use if you are

    taking sedatives or tranquilizers.

    When using this product

    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

    adults and children 12 years and over1 to 2 tablets
    children 6 to under 12 years
    		1 tablet
    children under 6 years
    		do not use
  • Other information

  • Inactive ingredients

    corn starch, D&C red #27 aluminum lake, dibasic calcium phosphate dihydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polyvinyl alcohol, silicon dioxide, stearic acid, talc, titanium dioxide

  • Questions or comments?

    1-800-426-9391

  • Principal Display Panel

    ♥︎CVS™

    NDC 59779-923-12

    Allergy Relief

    DIPHENHYDRAMINE HCl, 25 mg, Antihistamine

    Compare to Benadryl® Allergy ULTRATABS® Tablets*

    Relief of: Itchy & watery eyes,
    Runny nose, Itchy throat,
    Sneezing

    100
    TABLETS

    Actual Size

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED
    SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    *This product is not manufactured or distributed by
    Kenvue Inc., owner of the registered trademark
    Benadryl® Allergy ULTRATABS® .

    50844
    ORG072132912

    Distributed by: CVS Pharmacy, Inc.
    One CVS Drive, Woonsocket, RI 02895
    © 2025 CVS/pharmacy
    CVS.com® 1-800-SHOP CVS
    V-18615

    100% money back
    guaranteed.
    CVS.com/return policy

    CVS 44-329

    CVS 44-329

  • INGREDIENTS AND APPEARANCE
    ALLERGY RELIEF 
    diphenhydramine hcl tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-923
    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
    STARCH, CORN (UNII: O8232NY3SJ)  
    D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TALC (UNII: 7SEV7J4R1U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeOVALSize11mm
    FlavorImprint Code 44;329
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59779-923-031 in 1 PACKAGE03/02/1990
    110 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:59779-923-082 in 1 CARTON03/02/1990
    212 in 1 BLISTER PACK; Type 0: Not a Combination Product
    3NDC:59779-923-224 in 1 CARTON03/02/1990
    312 in 1 BLISTER PACK; Type 0: Not a Combination Product
    4NDC:59779-923-121 in 1 CARTON03/02/1990
    4100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    5NDC:59779-923-51365 in 1 BOTTLE; Type 0: Not a Combination Product03/02/1990
    6NDC:59779-923-071 in 1 CARTON03/02/199007/08/2018
    636 in 1 BLISTER PACK; Type 0: Not a Combination Product
    7NDC:59779-923-061 in 1 CARTON03/02/199006/16/2025
    7200 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01203/02/1990
    Labeler - CVS Pharmacy (062312574)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.038154464pack(59779-923)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867837manufacture(59779-923) , pack(59779-923)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.832867894manufacture(59779-923)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.868734088manufacture(59779-923)
    Establishment
    NameAddressID/FEIBusiness Operations
    LNK International, Inc.967626305pack(59779-923)