Label: ACTIDOGESIC- dexbrompheniramine maleate, acetaminophen tablet

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 December 4, 2018

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • ACTIVE INGREDIENT

    Active Ingredients in each caplet:Dexbrompheniramine Maleate 1 mg, Acetaminophen 1mg

  • PURPOSE

    Antihistamine, Pain reliever/fever reducer

  • INDICATIONS & USAGE

    Uses

    • For the temporary relief of minor aches and pains associated with • headache

    • muscular aches • backaches • minor arthritis pain • common cold • toothaches • menstrual

    cramps • temporarily reduces fever • itchy and watery eyes due to hay fever.

  • WARNINGS

    Warnings

    Liver Warning:

    This product contains acetaminophen. Severe liver damage may occur if you take • more than 8 caplets (4,000 mg) in 24 hours, which is the maximum daily amount • with other drugs containing acetaminophen • 3 or more alcoholic drinks every day while using this product

    Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: • skin reddening • blisters • rash

    Caution: May cause drowsiness; alcohol, sedatives, and tranquilizers may increase the

    drowsiness effect. Avoid alcoholic beverages while taking this product. Use caution when

    driving a motor vehicle or operating machinery. Do not take this product if you are taking

    sedatives or tranquilizers, without first consulting your doctor.

  • ASK DOCTOR

    Ask a doctor before use

    • if you have liver disease • if you are taking the blood thinning drug warfarin.

    Stop using this product and ask a doctor if

    • pain gets worse or lasts more than 10 days • fever gets worse or lasts more than 3 days

    • new symptoms occur • redness or swelling is present • These could be signs of a serious condition.

  • DO NOT USE

    Do not use

    • with any other drug containing acetaminophen (prescription or nonprescription) this will provide more than the recommended dose (overdose) of acetaminophen and could cause serious health concerns. If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist • if you are allergic to acetaminophen or any of the inactive ingredients in the product • for more than 10 days for pain, unless directed by a doctor.

    Do not take this product, unless directed by a doctor, if you have a breathing problem such as emphysema or chronic bronchitis, if you have glaucoma or difficulty in urination due to enlargement of the prostate gland.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • OVERDOSAGE

    In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

  • DOSAGE & ADMINISTRATION

    Directions • Do not exceed recommended dosage

    Adults and children 12 years of age and older:

    Take 2 caplets every 4 to 6 hours as needed, do not exceed 8 caplets in 24 hours, or as directed by a doctor, do not use for more than 10 days

    unless directed by a doctor.

    Children under 12 years of age:

    Do not use.

  • OTHER SAFETY INFORMATION

    Other Information

    • Tamper Evident. Do not use if inner seal is torn, broken, or missing

    • Store at controlled room temperature 15°- 30°C (59°- 86°F)

    • Avoid excessive heat or humidity

  • INACTIVE INGREDIENT

    Inactive Ingredients: FD&C Red #40, FD&C Yellow #6, hypromellose, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate, starch, stearic acid, and titanium dioxide

  • PRINCIPAL DISPLAY PANEL

    actidogesic

  • INGREDIENTS AND APPEARANCE
    ACTIDOGESIC 
    dexbrompheniramine maleate, acetaminophen tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63102-402
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE1 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
    POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColororangeScore2 pieces
    ShapecapsuleSize17mm
    FlavorImprint Code A402
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63102-402-10100 in 1 BOTTLE; Type 0: Not a Combination Product10/14/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34110/14/2016
    Labeler - ACTIPHARMA, INC (079340948)
    Registrant - ACTIPHARMA, INC (079340948)