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Acetaminophen by Cardinal Health

Medically reviewed on January 25, 2018

Dosage form: tablet
Ingredients: ACETAMINOPHEN 325mg
Labeler: Cardinal Health
NDC Code: 55154-5842

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Acetaminophen, USP 325 mg

Active ingredient

Drug Facts

See new warning information.

Acetaminophen 325 mg

Purpose

Pain reliever/fever reducer

Keep Out of Reach of Children

Keep out of the reach of children.

Uses

To reduce fever and for the temporary relief of minor aches and pains due to headache, backache, the common cold, muscular aches, minor pain of arthritis, toothache, premenstrual and menstrual cramps. Temporarily reduces fever.

Warnings

This package is intended for institutional use only. If pregnant or breast-feeding, ask a health professional before use. This unit dose package is not child-resistant. If dispensed for outpatient use, a child-resistant container should be utilized.

TAMPER-EVIDENT: Each tablet is individually sealed. Do not use if blister is torn or broken.

Liver warning: This product contains acetaminophen. Severe liver damage may occur if

  • adult takes more than 12 tablets in 24 hours, which is the maximum daily amount
  • child takes more that 5 doses in 24 hours.
  • taken with other drugs containing acetaminophen
  • adult has 3 or more alcoholic drinks everyday while using this product

Ask a doctor before use if the user has liver disease.

Do not use 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 or pharmacist before use if the user is taking the blood thinning drug warfarin.

Stop use and ask a doctor if

  • pain gets worse or lasts more than 10 days in adults and children
  • pain gets worse or lasts more than 5 days in children under 12 years
  • 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.

Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222). Quick 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 tablets every 4 to 6 hours while symptoms last
  • do not take more than 12 tablets in 24 hours.
children 6 to 11 years
  • take 1 tablet every 4 to 6 hours while symptoms last
  • do not take more than 5 tablets in 24 hours.
children under 6 yearsDo not use adult regular strength products in children under 6 years of age: this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage.

Inactive ingredients

povidone starch, stearic acid

Storage

Store at Controlled Room Temperature 15-30 C (59-86 F)

Protect from moisture, heat and light

Questions? Call 1-888-838-2872, weekdays,

8 AM - 5 PM Eastern Time

Manufactured for:

GOLDLINE LABORATORIES, INC.

Sellersville, PA 18960

by: LNK International, Inc.

Hauppauge, NY 11788

Repackaged by Cardinal Health

Zanesville, OH 43701

Principal Display Panel

Acetaminophen Tablets USP

325 mg

10 Tablets

ACETAMINOPHEN 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-5842(NDC:0182-8447)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE 
STARCH, CORN 
STEARIC ACID 
Product Characteristics
ColorWHITEScore2 pieces
ShapeROUNDSize10mm
FlavorImprint Code44;104
Contains    
Packaging
#Item CodePackage Description
1NDC:55154-5842-010 BLISTER PACK in 1 BAG
11 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other06/02/2011
Labeler - Cardinal Health (188557102)
Establishment
NameAddressID/FEIOperations
Cardinal Health188557102REPACK(55154-5842)

 
Cardinal Health

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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