Label: EQUATE ALLERGY RELIEF- diphenhydramine hydrochloride tablet 

  • Label RSS
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 11/11

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

  • Active ingredient (in each tablet)

    Diphenhydramine hydrochloride 25 mg

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  • Purpose

    Antihistamine

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  • Uses

    • temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
    • runny nose
    • sneezing
    • itchy, watery eyes
    • itchy nose or throat
    • temporarily relieves these symptoms of the common cold:
    • runny nose
    • sneezing
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  • Warnings

    Do not use

    • with any other product containing diphenhydramine, even one used on skin
    • to make a child sleepy

    Ask a doctor before use if you have

    • glaucoma
    • trouble urinating due to an enlarged prostate gland
    • a breathing problem such as emphysema or chronic bronchitis

    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
    • 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.

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  • Directions

    • take every 4 to 6 hours, not more than 6 doses in 24 hours
    adults and children 12 years of age and over 1 or 2 tablets
    children 6 to under 12 years of age 1 tablet
    children 4 to under 6 years of age do not use unless directed by a doctor
    children under 4 years of age do not use
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  • Other information

    • each tablet contains: calcium 20 mg
    • store at 20°-25°C
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  • Inactive ingredients

    carnauba wax, crospovidone, D&C red no. 27 aluminum lake, dibasic calcium phosphate, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, starch, stearic acid, titanium dioxide

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  • Questions or comments?

    1-888-287-1915

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  • Principal Display Panel

    Compare to Benadryl® Allergy Ultratab® Active Ingredient

    Allergy Relief

    Diphenhydramine HCl 25 mg

    Antihistamine

    Easy to Swallow

    Relieves:

    Sneezing

    Itchy, watery eyes

    Runny nose

    Itchy throat

    25 mg

    Actual Size

    Allergy Relief Carton Image 1

    Allergy Relief Carton Image 1

    Allergy Relief Carton Image 2

    Allergy Relief Carton Image 2

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  • INGREDIENTS AND APPEARANCE
    EQUATE ALLERGY RELIEF 
    diphenhydramine hydrochloride tablet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:49035-479
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE) DIPHENHYDRAMINE HYDROCHLORIDE 25 mg
    Inactive Ingredients
    Ingredient Name Strength
    CARNAUBA WAX  
    CROSPOVIDONE  
    HYPROMELLOSES  
    MAGNESIUM STEARATE  
    CELLULOSE, MICROCRYSTALLINE  
    POLYETHYLENE GLYCOLS  
    POLYSORBATE 80  
    STEARIC ACID  
    TITANIUM DIOXIDE  
    DIBASIC CALCIUM PHOSPHATE DIHYDRATE  
    Product Characteristics
    Color PINK (dark) Score no score
    Shape CAPSULE Size 10mm
    Flavor Imprint Code L479
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49035-479-78 1 in 1 CARTON
    1 100 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part341 07/30/1999
    Labeler - Wal-Mart Stores Inc (051957769)
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