Label: CIRCLE K ALLERGY ANTIHISTAMINE- diphenhydramine hydrochloride tablet, film coated

  • NDC Code(s): 66715-5554-2, 66715-5554-3, 66715-5654-2, 66715-5654-3
  • Packager: Lil' Drug Store Products, Inc.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated December 14, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • 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
      • 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

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

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

    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 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 overtake 1 to 2 tablets
    children 6 to under 12 yearstake 1 tablet
    children under 6 yearsdo not use
  • Other information

    • each tablet may contain: calcium 25 mg
    • store at room temperature 68°-77°F (20°-25°C)
    • protect from light and moisture
  • Inactive ingredients

    carnauba wax 1, colloidal silicon dioxide, croscarmellose sodium, D&C red #27, dicalcium phosphate 1, hypromellose, lactose 1, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80 1, titanium dioxide

    1
    may contain
  • Questions or comments?

    Call toll-free 1-877-507-6516 (M-F 8AM – 4:30PM CST)

  • SPL UNCLASSIFIED SECTION

    Proudly distributed by Circle K Stores Inc.

  • PRINCIPAL DISPLAY PANEL - 4 Tablet Pouch Carton - NDC 66715-5654-2

    Compare to the Active Ingredient
    in Benadryl® Allergy**

    CIRCLE K™

    Allergy

    Diphenhydramine HCl 25 mg, Antihistamine

    ACTUAL SIZE

    Relieves

    • Runny Nose - Sneezing
    • Itchy, Watery Eyes
    • Itchy Nose or Throat

    4 Tablets
    2 POUCHES, 2 TABLETS PER POUCH

    PRINCIPAL DISPLAY PANEL - 4 Tablet Pouch Carton - NDC 66715-5654-2
  • PRINCIPAL DISPLAY PANEL - 6 Tablet Pouch Carton - NDC 66715-5554-3

    RELIEVES SYMPTOMS OF HAY FEVER & OTHER ALLERGIES
    Compare to the active ingredient in
    Benadryl® Allergy ULTRATABS®**

    CIRCLE K™

    multi-symptom

    allergy

    Diphenhydramine HCl 25 mg,

    Antihistamine

    [tablet image]

    actual size

    6 tablets (2 per pouch)

    PDP/Package

  • INGREDIENTS AND APPEARANCE
    CIRCLE K ALLERGY  ANTIHISTAMINE
    diphenhydramine hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5654
    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
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeOVALSize11mm
    FlavorImprint Code 061;T
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-5654-22 in 1 CARTON10/17/201604/14/2024
    12 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:66715-5654-33 in 1 CARTON10/15/201904/14/2024
    22 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/01/201404/14/2024
    CIRCLE K ALLERGY  ANTIHISTAMINE
    diphenhydramine hydrochloride tablet, film coated
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5554
    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
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeOVALSize11mm
    FlavorImprint Code 048;D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66715-5554-22 in 1 CARTON10/17/201604/14/2024
    12 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:66715-5554-33 in 1 CARTON10/15/2019
    22 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01211/01/2014
    Labeler - Lil' Drug Store Products, Inc. (093103646)
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