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

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Pain Relief

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

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient

Acetaminophen 500 mg

Purpose

Analgesic/Antipyretic

Pain Relief 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 caplets 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 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.

Directions

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

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.

Other Information

store at room temperature
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 glycolates.

Package/Label Principal Display Panel

Pain Relief

Acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:62211-012
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
STARCH, CORN
HYPROMELLOSE 2208 (100 MPA.S)
POLYETHYLENE GLYCOLS
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:62211-012-40 40 in 1 BOTTLE
2 NDC:62211-012-10 100 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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