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Manufacturer:A&z Pharmaceutical, Inc.
Category:Over-the-counter (OTC) Marketed Drugs

Acetaminophen Tablets, 500mg

ACETAMINOPHEN  - acetaminophen tablet 
A&Z Pharmaceutical, Inc.

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.


Acetaminophen Tablets, 500mg


Temporary relief of minor aches and pains associated with ■ common cold ■ headache ■ toothache ■ muscular aches ■ backache ■ arthritis ■ menstrual cramps ■ and reduction of 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

Ask a Doctor

before use if user has liver disease

Ask a Doctor/Pharmacist before use if you

are taking the blood thinning drug warfarin

Stop Use and ask a doctor if

■ symptoms do not improve ■ pain gets worse or lasts for more than 10 days ■ fever gets worse or lasts for more than 3 days ■ new symptoms occur ■ redness or swelling is present ■ a rare sensitivity reaction occurs ■ You may report side effects to 1-888-952-0050

If pregnant or breast-feeding,

ask a health professional before use

Keep Out of Reach of Children.

In case of accidental overdose, contact a doctor or Poison Control Center immediately. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms. Do not exceed recommended dosage.


Adults and children 12 years of age and older: take 2 tablets every 4 to 6 hours as needed. Do not take more than 8 tablets in 24 hours;

Children under 12 years of age: do not use this regular strength product. This will provide more than the recommended dose (overdose) and could cause serious health problems.

Other information

■ store at room temperature 59º-86º F (15º-30º C) ■ do not use if imprinted safety seal under cap is broken or missing

Inactive ingredients

corn starch, pregelatinized starch, stearic acid. May contain povidone and sodium starch glycolate.


picture of label

acetaminophen tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:62211-011(NDC:011)
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Product Characteristics
Color white Score no score
Shape ROUND Size 12mm
Flavor Imprint Code AZ011
# Item Code Package Description Multilevel Packaging
1 NDC:62211-011-99 27000 TABLET ( TABLET) in 1 CARTON None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part343 03/16/2004

Labeler - A&Z Pharmaceutical, Inc. (926820705)
Registrant - A&Z Pharmaceutical, Inc. (926820705)

Revised: 04/2010 A&Z Pharmaceutical, Inc.

Reproduced with permission of U.S. National Library of Medicine

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