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

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Acetaminophen

Physicians Total Care, Inc.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredients

Acetaminophen 500 mg

Purpose

Pain Reliever/Fever Reducer

Acetaminophen Uses

  • temporarily relieves minor aches and pains
  • temporarily reduces fever

Warnings

Liver warning:
  • 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
Ask a doctor or pharmacist before use if you are

Stop use and ask a doctor if

  • pain gets worse or lasts more than 10 days
  • fever gets worse or lasts more than 3 days
  • new symptom occur
  • redness or swelling is present


If pregnant or breast-feeding,


Overdose Warning:

Keep out of reach of children.

Directions

  • do not take more than directed
  • adults and children 12 years and over: take 1-2 tablets every 4-6 hours, as needed; not more than 8 tablets in 24 hours
  • children under 12 years: do not use

Other Information

  • TAMPER EVIDENT: Do not use if imprinted seal under cap is missing or broken.
  • store at 20⁰C-25⁰C (68⁰F-77⁰F)
  • for institutional use only

Inactive Ingredients

povidone, sodium starch glycolate, starch stearic acid. May also contain: crospovidone, methylparaben and probylparaben


NDC 54868-2457-2

Acetaminophen

SEE NEW WARNINGS

Non-Aspirin

Extra Strength

PAIN RELIEF

Acetaminophen Tablets

*Compare to active ingredient in Extra Strength Tylenol Tablets

PACKAGE NOT CHILD RESISTANT

500 mg each

Dist. By: Gericare Pharmaceuticals Corp.










Acetaminophen

Acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54868-2457(NDC:57896-201)
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
povidone
SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID
CROSPOVIDONE
METHYLPARABEN
PROPYLPARABEN

Product Characteristics

Color Size Imprint Code Shape
white (WHITE) 12 mm M2A457344 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:54868-2457-2 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2002-08-22


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