Label: ACETAMINOPHEN tablet

  • NDC Code(s): 70010-161-01, 70010-161-05, 70010-161-10
  • Packager: Granules Pharmaceuticals Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 2, 2025

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

  • ACTIVE INGREDIENT (IN EACH CAPLET)
    Acetaminophen, USP 500 mg
  • PURPOSE
    Pain reliever/fever reducer
  • USES
    • temporarily relieves minor aches and pains due to: • the common cold - • headache - • backache - • minor pain of arthritis - • toothache - • muscular aches - • premenstrual ...
  • WARNINGS
    Liver warning: This product contains acetaminophen. Severe Liver damage may occur if you take - • more than 4,000 mg of acetaminophen 24 hours. • with other drugs containing ...
  • Do not use
    • with any other drugs containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. • if you are ...
  • Ask a doctor before use if you have
    liver disease.
  • Ask a doctor or pharmacist before use if you are
    taking the blood thinning drug warfarin.
  • Stop use and ask 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 ...
  • If pregnant or breast-feeding
    ask a health professional before use.
  • Keep out of reach of children
    Over dose warning: In case of overdose, get medical help or Contact Poison Control Center right away. (1-800-222-1222) Quick medical attention is critical for adults as well as for children even ...
  • DIRECTIONS
    • do not take more than directed (see overdose warning) adults and children - 12 years and over - • take 2 caplets every 6 hours while symptoms last - • do not take ...
  • OTHER INFORMATION
    • store at 20-25°C (68-77°F). See USP Controlled Room Temparature - • avoid high humidity - • See end panel for lot number and expiration date
  • INACTIVE INGREDIENTS
    hydroxyethyl methyl cellulose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate, stearic acid.
  • QUESTIONS OR COMMENTS ?
    Contact - 1-877-770-3183 Mon-Fri 8:00 AM EST to 5:00 PM PST. +All trademarkes are property of their reapective owners. This product is not affliated with the makers/owners of - Extra Strength ...
  • PRINCIPAL DISPLAY PANEL
    100-count-bottle-label ...
  • INGREDIENTS AND APPEARANCE
    Product Information