Label: G-DOLOGEN- acetaminophen, dexbrompheniramine maleate tablet

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

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 14, 2018

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

  • Drug Facts

  • Active Ingredients (in each caplet)

    Acetaminophen 650 mg

    Dexbrompheniramine Maleate 2 mg

  • Purpose

    Analgesic, Antipyretic (Fever Reducer)

    Antihistamine

  • Uses:

    temporarily relieves minor aches and pains due to: • headache • common cold • toothache • backache • muscular aches • menestrual cramps • minor pain of arthritis • relieves runny nose, and sneezing, itching of the nose or throat, and itchy, watery eyes due to hay fever or other respiratory allergies. Temporarily reduces fever.

  • Warnings:

    Liver Warning: This product contains acetaminophen. Severe liver damage may occur if you take: • more than 6 caplets (3,900 mg) in 24 hours • with other drugs containing acetaminophen • 3 or more alcoholic drinks while using this product.

    Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: • skin reddening • blisters • rash. If skin reaction occurs, stop use and seek medical help right away.

    Do not use : with any other product 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. When using this product do not exceed recommended dose.

    Ask a doctor before use if you have: • liver disease • breathing problems such as emphysema or chronic bronchitis • glaucoma or difficulty in urination due to enlargement of the prostate gland.

    Ask a doctor or pharmacist before use if you are taking • the blood thinning drug warfarin • sedatives or tranquilizers.

    While using this product: • excitability may occur • drowsiness may occur; 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.

    Stop use and ask a doctor if: • pain gets worse or lasts for more than 10 days • fever gets worse or lasts for more than 3 days • new symptoms occur • redness or swelling is present. These could be signs of a serious condition.

    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. (1-800-222-122) Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • Directions:

    Adults and children 12 years of age and older:Take 1 caplet every 4-6 hours, or directed by a doctor. Do not exceed 6 caplets in 24 hours.
    Children under 12 years: consult doctor.

  • Other Information:

    • Tamper Evident. Do not use if seal is broken.

    • Store at controlled room temperature 15° to 30° C (59° to 86°F). • Avoid excessive heat and humidity.

  • Inactive Ingredients:

    corn starch, hydroxypropylmethylcellulose, maltodextrin, microcrystalline cellulose, polyethylene glycol, povidone, sodium starch glycolate and stearic acid.

  • SPL UNCLASSIFIED SECTION

    Compare to Dologen®

    Pain Reliever

    Fever Reducer

    Antihistamine

    Sugar & Dye Free

    Manufactured in the USA for:

    Kramer-Novis, San Juan, PR 00917. Tel: (787) 767-2072

    www.kramernovis.com

  • Packaging

    G-dolo

  • INGREDIENTS AND APPEARANCE
    G-DOLOGEN 
    acetaminophen, dexbrompheniramine maleate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52083-681
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DEXBROMPHENIRAMINE MALEATE (UNII: BPA9UT29BS) (DEXBROMPHENIRAMINE - UNII:75T64B71RP) DEXBROMPHENIRAMINE MALEATE2 mg
    ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    POVIDONE K30 (UNII: U725QWY32X)  
    SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    Colorwhite (IVORY WHITE) Score2 pieces
    ShapeCAPSULE (D) Size19mm
    FlavorImprint Code D
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52083-681-9090 in 1 BOTTLE; Type 0: Not a Combination Product08/27/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34108/27/2014
    Labeler - KRAMER NOVIS (090158395)
    Registrant - KRAMER NOVIS (090158395)