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Regular Strength Pain Relief by NuCare Pharmaceuticals, Inc.

Dosage form: tablet
Ingredients: ACETAMINOPHEN 325mg
Labeler: NuCare Pharmaceuticals, Inc.
NDC Code: 66267-003

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.

Active Ingredients

Acetaminophen 325 mg


Pain Reliever/Fever Reducer


  • temporarily relieves minor aches and pains
  • temporarily reduces fever


Liver warning:

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

  • more than 12 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.

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 symptom 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.

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

Keep out of reach of children.

  • do not take more than directed
  • adults and children 12 years and over: take 2 tablets every 4-6 hours, as needed; not more than 12 tablets in 24 hours
  • children under 12 years: ask a doctor

Other Information
  • TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.
  • store at 20⁰C-25⁰C (68⁰F-77⁰F)
  • for institutional use only

Inactive Ingredients

povidone, sodium starch glycolate, starch stearic acid. May also contain: crospovidone, methylparaben and probylparaben

Package Label

Dist. by: Gericare Pharmaceuticals Corp.

1650 63rd street

Brooklyn, NY 11204

acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66267-003(NDC:57896-101)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
Product Characteristics
Colorwhite (WHITE) Score2 pieces
ShapeROUND (Round) Size10mm
FlavorImprint CodeM2A357344
#Item CodePackage Description
1NDC:66267-003-2020 TABLET in 1 BOTTLE
2NDC:66267-003-2424 TABLET in 1 BOTTLE
3NDC:66267-003-2525 TABLET in 1 BOTTLE
4NDC:66267-003-3030 TABLET in 1 BOTTLE
5NDC:66267-003-5050 TABLET in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34309/16/2016
Labeler - NuCare Pharmaceuticals, Inc. (010632300)
NuCare Pharmaceuticals, Inc.010632300repack(66267-003)

Revised: 09/2016
NuCare 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.