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

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Pain Relief Extra Strength

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Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredients


Purpose

Analgesic, Antipyretic

Directions: 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 extra strength product; this
will provide more than the recommended dose (overdose) and
could cause serious health problems.

Uses

Uses: • temporary relief of minor aches and pains associated with
• common cold • headache • backache • arthritis • toothache •
muscular aches • 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 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 for more than 10 days • a
rare sensitivity reaction occurs • fever gets worse or lasts more
than 3 days • symptoms do not improve • new symptoms occur •
redness or swelling is present. You may report side effects to
888-952-0050.

If pregnant or breast-feeding, ask a health
professional before use.

KEEP OUT OF REACH OF CHILDREN.

Inactive ingredients: corn starch, hydoxypropyl methylcellulose,
polyethylene glycol, pregelatinized starch, stearic acid, titanium
dioxide. May contain povidone and sodium starch glycolate

MM1

Pain Relief Extra Strength

Pain Relief Extra Strength

Acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52904-446
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
POLYETHYLENE GLYCOL 300
STEARIC ACID
titanium dioxide
SODIUM STARCH GLYCOLATE TYPE A POTATO
POVIDONE K29/32

Product Characteristics

Color Size Imprint Code Shape
white (snow white) 12 mm AZ235 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52904-446-02 2 in 1 PACKET

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2012-10-15


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