Label: ARTHRITISPAIN RELIEF- acetaminophen tablet

  • NDC Code(s): 59726-669-10
  • Packager: P & L Development, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated November 1, 2024

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  • Active ingredient (in each caplet)
    Acetaminophen 650 mg
  • Purpose
    Pain reliever/fever reducer
  • Uses
    temporarily relieves minor aches and pains due to: minor pain of arthritis - backache - muscular aches - toothache - premenstrual and menstrual cramps - headache - the common cold - temporarily reduces ...
  • Warnings
    Liver warning:  This product contains acetaminophen. Severe liver damage may occur if you take: more than 6 caplets in 24 hours, which is the maximum daily amount - with other drugs containing ...
  • Directions
    do not take more than directed (see Overdose warning) adults - take 2 caplets every 8 hours with water - swallow whole; do not crush, chew, split or dissolve - do not take more than 6 caplets in ...
  • Other information
    store between 20-25°C (68-77°F)
  • Inactive ingredients
    D&C yellow #10 aluminum lake, FD&C yellow #6 aluminum lake, hydroxyethyl cellulose, magnesium stearate, maize starch, microcrystalline cellulose, povidone, pregelatinized starch, sodium lauryl ...
  • Questions or comments?
    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
  • Principal Display Panel
    Compare to the active ingredient of Tylenol® 8HR Arthritis Pain† extended-release - arthritis pain reliever - acetaminophen 650 mg - pain reliever/fever reducer - for the temporary relief of ...
  • Product Label
    READYinCASE Arthritis Pain Reliever
  • INGREDIENTS AND APPEARANCE
    Product Information