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Pharbetol by Preferred Pharmaceuticals, Inc.

Medically reviewed on May 22, 2018

Dosage form: tablet
Ingredients: ACETAMINOPHEN 500mg
Labeler: Preferred Pharmaceuticals, Inc.
NDC Code: 68788-6408

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 Facts

Active ingredient (in each tablet)

Acetaminophen 500mg


Pain reliever/fever reducer


Temporarily relieves minor aches and pains due to:

minor pain of arthritis
muscular aches
menstrual cramps

Temporarily reduces fever


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

more than 8 tablets in 24 hours, which is the maximum daily amount
with other drugs containing acetaminophen
3 or more alcoholic drinks every day while using this product

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
if you are allergic to acetaminophen or any of the inactive ingredients in this product

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.

Overdose warning:

Taking more than the recommended dose (overdose) may cause liver damage. In the case of overdose, get medical help or contact a Poison Control Center right away.

do not take more than directed (see overdose warning).
Adult and Children 12 years and over: take 2 tablets, every 4 to 6 hours while symptoms last. Do not take more than 8 tablets in 24 hours. Do not take for more than 10 days unless directed by a doctor.
Children under 12 years: do not use adult extra strength product in children under 12 years of age; this will provide more than recommended dose (overdose) and may cause liver damage.

Inactive ingredients

Povidone, Pregelatinized corn starch, sodium starch glycolate, stearic acid.


Adverse drug event call: (866) 562-2756

acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-6408(NDC:16103-376)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
ColorwhiteScoreno score
FlavorImprint CodePH044
#Item CodePackage Description
1NDC:68788-6408-220 TABLET in 1 BOTTLE, PLASTIC
2NDC:68788-6408-330 TABLET in 1 BOTTLE, PLASTIC
3NDC:68788-6408-445 TABLET in 1 BOTTLE, PLASTIC
4NDC:68788-6408-550 TABLET in 1 BOTTLE, PLASTIC
5NDC:68788-6408-1100 TABLET in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34306/08/2016
Labeler - Preferred Pharmaceuticals, Inc. (791119022)
Registrant - Preferred Pharmaceuticals, Inc. (791119022)
Preferred Pharmaceuticals, Inc.791119022REPACK(68788-6408)

Preferred Pharmaceuticals, Inc.

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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.