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Pain Reliever (acetaminophen 500 mg) Dailymed

  1. Human OTC
  2. Non-opioid Analgesics
  3. L.N.K. International, Inc.

Generic: acetaminophen is used for the treatment of Fever Glucosephosphate Dehydrogenase Deficiency Liver Diseases Pain

Pain Reliever tablet, coated - (acetaminophen 500 mg) image
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IMPRINT: L 5     SHAPE: capsule
    COLOR: blue

All Imprints

acetaminophen 500 mg oral tablet - l 5 capsule red

acetaminophen 500 mg - l 5 capsule blue

acetaminophen 500 mg - l 5 oval

  1. FDA Adverse Reactions

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Active Ingredient (in Each Gelcap)


Acetaminophen 500 mg

Purpose


Pain reliever/fever reducer

Uses

  • temporarily relieves minor aches and pains due to:
    • headache
    • the common cold
    • backache
    • minor pain of arthritis
    • toothache
    • muscular aches
    • premenstrual and menstrual cramps
  • temporarily reduces fever

Warnings


Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take
  • more than 4,000 mg of acetaminophen in 24 hours
  • 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
  • bulers
  • rash

If a skin reaction occurs, stop use and seek medical help right away.

Do not use

  • if you are allergic to acetaminophen or any of the inactive ingredients in this product
  • with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.

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 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.

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. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

  • do not take more than directed
  • adults and children 12 years and over
    • take 2 gelcaps every 6 hours while symptoms last
    • do not take more than 6 gelcaps in 24 hours, unless directed by a doctor
    • do not take for more than 10 days unless directed by a doctor
  • children under 12 years: ask a doctor

Other Information

  • store at 25ºC (77ºF); excursions permitted between 15º-30ºC (59º-86ºF)
  • avoid high humidity
  • see end flap for expiration date and lot number

Inactive Ingredients


croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, stearic acid, titanium dioxide

Questions Or Comments?


1-800-426-9391

Principal Display Panel


QUALITY+PLUS

NDC 50844-519-21

*Compare to active ingredientin Extra Strength Tylenol®Rapid Release Gels

EXTRA STRENGTHPAIN RELIEVERAcetaminophen 500 mg PAIN RELIEVER/FEVER REDUCER

16 Gelcaps

CONTAINS NO ASPIRIN

ACTUALSIZE

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

*This product is not manufactured or distributedby Johnson & Johnson Corporation, owner of theregistered trademark Extra Strength Tylenol®Rapid Release Gels.    50844  ORG032251921

Distributed by LNK INTERNATIONAL, INC. 60 Arkay DriveHauppauge, NY 11788USA
Quality Plus 44-519

DISCLAIMER:

"This tool does not provide medical advice, and is for informational and educational purposes only, and is not a substitute for professional medical advice, treatment or diagnosis. Call your doctor to receive medical advice. If you think you may have a medical emergency, please dial 911."

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"This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product."

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