Label: CHLORTABS- chlorpheniramine maleate tablet

  • 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 04/15

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

  • Active ingredient (in each tablet)

    Chlorpheniramine maleate 4 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
      • itchy, watery eyes
      • sneezing
      • itching of the nose or throat
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  • Warnings

    Do not use

     to make a child sleepy.

    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 sedatives or tranquilizers.

    When using this product

    • drowsiness may occur
    • avoid alcoholic beverages
    • alcohol, sedatives, and tranquilizers may increase drowsiness
    • use caution 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.

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  • Directions

    adults and children 12 years of age and over 1 tablet every 4 to 6 hours.  Do not take more than 6 tablets in 24 hours.
    children 6 to under 12 years of age 1/2 tablet (break tablet in half) every 4 to 6 hours. Do not exceed 3 whole tablets in 24 hours.
    children under 6 years of age do not use this product in children under 6 years of age

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  • Other information

    • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
    • protect from excessive moisture
    • see end flap for expiration date and lot number
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  • Inactive ingredients

    corn starch, D&C yellow #10 aluminum lake, lactose anhydrous, magnesium stearate, microcrystalline cellulose

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  • Questions or comments?

    1-888-287-1915 

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  • Principal Display Panel

    equate™

    NDC 49035-940-12

    Compare to
    Chlor-Trimeton®
    Allergy Tablets
    Active
    Ingredient*

    ChlorTabs
    Chlorpheniramine Maleate 4 mg
    Antihistamine / Allergy Relief

    Relieves:
    • Sneezing   •Itchy, watery eyes
    • Runny nose   • Itchy throat

    100
    TABLETS

    Actual Size

    4
    HOUR
    RELIEF

    Satisfaction guaranteed - Or we'll replace it or give you your money back. For questions or comments or to report an undesired reaction or side effect, please call 1-888-287-1915.

    Distributed by: Wal-Mart Stores, Inc.,
    Bentonville, AR 72716

    *This product is not manufactured or distributed by MSD Consumer Care, Inc., owner of the registered trademark Chlor-Trimeton® Allergy Tablets.
    50844   REV0213E19412

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

    Equate 44-194

    Equate 44-194

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  • INGREDIENTS AND APPEARANCE
    CHLORTABS 
    chlorpheniramine maleate tablet
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-940
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U) CHLORPHENIRAMINE MALEATE 4 mg
    Inactive Ingredients
    Ingredient Name Strength
    ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    Product Characteristics
    Color YELLOW Score 2 pieces
    Shape ROUND Size 8mm
    Flavor Imprint Code 44;194
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:49035-940-12 1 in 1 CARTON
    1 100 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH FINAL part341 12/19/1992
    Labeler - Wal-Mart Stores Inc (051957769)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 832867894 MANUFACTURE(49035-940)
    Establishment
    Name Address ID/FEI Business Operations
    LNK International, Inc. 038154464 PACK(49035-940)
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