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

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Pain Relief

American Sales Company
A&Z Pharmaceutical, Inc.

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Acetaminophen 500 mg

Analgesic/Antipyretic

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 takemore than 4000mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day while using this product

with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist

liver disease

are taking the blood thinning drug warfarin

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

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 caplets (1,000 mg) every 6 hours while symptoms last. Do not take more than 6 caplets (3,000 mg) in 24 hours, unless directed by a doctor.

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

store at room temperature

do not use if imprinted safety seal under cap is broken or missing

corn starch, hydroxypropyl methylcellulose, polyethylene glycol, pregelatinized starch, stearic acid, titanium dioxide. May contain povidone, and sodium starch glycolates.

Package/Label Principal Display Panel

Pain Relief

Acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41520-012
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 500 mg

Inactive Ingredients

Ingredient Name Strength
HYPROMELLOSES
POLYETHYLENE GLYCOLS
STARCH, CORN
STEARIC ACID
titanium dioxide

Product Characteristics

Color Size Imprint Code Shape
WHITE 17 mm AZ012 CAPSULE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41520-012-24 24 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2014-06-10


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