Label: ADULT ALLERGY RELIEF DYE FREE- diphenhydramine hydrochloride solution

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

Drug Label Information

Updated November 11, 2024

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  • Drug Facts

    Active ingredient [in each 10 mL]

    Diphenhydramine HCl, USP 25 mg

  • Purpose

    Antihistamine

  • Uses

    ▪
    temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    ▪
    sneezing
    ▪
    itchy, watery eyes
    ▪
    runny nose
    ▪
    itching of the nose or throat
  • 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 chronic bronchitis
    ▪
    glaucoma
    ▪
    a sodium-restricted diet
    ▪
    trouble urinating due to enlarged prostate

    Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers

  • When using this product

    •
    marked drowsiness may occur
    •
    avoid alcoholic drinks
    •
    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

    In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    ▪
    measure only with dosing cup provided
    ▪
    Keep dosing cup with product
    ▪
    mL = milliliter
    ▪
    do not take more than 6 doses in 24 hours

     Age (yr)

    Dose (mL)

    Adult and children 12 years and older

    10 mL to 20 mL (2 to 4 tsp) every 4 to 6 hrs

    Children under 12 years

    Do not use
  • Other information

    •
    each 10 mL contains: sodium 6 mg
    •
    store at room temperature. Store in outer carton until contents used
    •
    do not refrigerate
    •
    see bottom panel for lot number and expiration date
    •
    protect from light
    •
    low sodium
  • Inactive ingredients

    anhydrous citric acid, carboxymethylcellulose sodium, flavors, glycerin, potassium citrate, purified water, sodium benzoate, sorbitol, sucralose

    Questions or Comments?

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  • Package Label-Principal Display Panel 4 Fl Oz (118 Ml Bottle)

    NDC 0363-7100-04

    Dye-Free

    AdultAllergyRelief

    Diphenhydramine HCl | Antihistamine

    For Relief of:

    •
    Runny nose
    •
    Itchy, watery eyes
    •
    Sneezing and Itchy Watery Eyes

    Sugar Free
    Cherry Flavor

    Naturally and Artificially Flavored

    4 FL OZ (118 mL)

    †Our pharmacists recommend the Walgreens brand.

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

    Walgreens

    100% SATISFACTION GURANTEED

    Walgreens.com

    @2021 Walgreens Co.

    IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING.


    Dye-Free Adult's Allergy Relief Diphenydramine HCl





  • INGREDIENTS AND APPEARANCE
    ADULT ALLERGY RELIEF  DYE FREE
    diphenhydramine hydrochloride solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-7100
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE25 mg  in 10 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    CHERRY (UNII: BUC5I9595W)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM CITRATE (UNII: EE90ONI6FF)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITOL (UNII: 506T60A25R)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorYELLOW (Colorless to Pale Yellow) Score    
    ShapeSize
    FlavorCHERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-7100-041 in 1 CARTON01/30/2020
    1118 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01201/30/2020
    Labeler - WALGREEN COMPANY (008965063)
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