Label: BENADRYL ALLERGY EXTRA STRENGTH LIQUI-GELS- diphenhydramine hydrochloride capsule, liquid filled

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2025

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    ​Drug Facts

  • Active ingredient (in each capsule)

    Diphenhydramine HCl 50 mg

  • Purpose

    Antihistamine

  • 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

    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

    • glaucoma
    • a breathing problem such as emphysema or chronic bronchitis
    • 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
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • be careful when driving a motor vehicle or operating machinery
    • excitability may occur, especially in children
    • avoid alcoholic drinks

    If pregnant or breast-feeding

    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 over1 capsule
    children under 12 yearsdo not use

  • Other information

    • store between 20-25°C (68-77°F). Avoid high humidity and excessive heat above 40°C (104°F). Protect from light.
    • do not use if blister unit is torn or broken
  • Inactive ingredients

    FD&C blue no. 1, gelatin, glycerin, polyethylene glycol, purified water, sorbitan, sorbitol

  • Questions or comments?

    call 1-877-717-2824 (toll-free) or 215-273-8755 (collect)

  • PRINCIPAL DISPLAY PANEL

    NEW

    NDC 50580-322-20

    Benadryl ®

    ALLERGY ®

    EXTRA STRENGHT

    LIQUI GELS ®*

    Diphenhydramine HCl 50 mg

    Antihistamine

    Sneezing

    Runny Nose

    Itchy, Watery Eyes

    Itchy Throat

    *liquid-filled capsules

    Actual Size

    20 CAPSULES

    benadryl_1.jpg

  • INGREDIENTS AND APPEARANCE
    BENADRYL ALLERGY EXTRA STRENGTH LIQUI-GELS 
    diphenhydramine hydrochloride capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50580-322
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HCL (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HCL50 mg
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SORBITAN (UNII: 6O92ICV9RU)  
    SORBITOL (UNII: 506T60A25R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    WATER (UNII: 059QF0KO0R)  
    GELATIN (UNII: 2G86QN327L)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    Product Characteristics
    ColorblueScoreno score
    ShapeOVALSize14mm
    FlavorImprint Code B50
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50580-322-202 in 1 CARTON05/15/202504/30/2027
    110 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01205/15/202504/30/2027
    Labeler - Kenvue Brands LLC (118772437)