Acetaminophen description, usages, side effects, indications, overdosage, supplying and lots more!

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Acetaminophen

A&Z Pharmaceutical, Inc.
A&Z Pharmaceutical, Inc.

Acetaminophen Tablets, 500mg


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

USES

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

WARNINGS

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

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.

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

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

DISPLAY PANEL

Acetaminophen

Acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62211-011(NDC:011)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 500 mg

Product Characteristics

Color Size Imprint Code Shape
white 12 mm AZ011 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:62211-011-99 27000 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2004-03-16


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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