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

Menu
Search

Acetaminophen

REMEDYREPACK INC.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

OTC - ACTIVE INGREDIENT

ACTIVE INGREDIENT



PURPOSES


USES

  • ●Headache
  • ●Muscular aches
  • ●Backache
  • ●Minor pain of arthritis
  • ●The common cold
  • ●Toothache
  • ●Premenstrual and menstrual cramps
  • ●Temporarily reduces fever.

WARNINGS

WARNINGS


  • ●adult takes more than 12 tablets in 24 hours, which is the maximum daily amount
  • ●child takes more than 5 doses in 24 hours
  • ●taken with other drugs containing acetaminophen
  • ●adult has 3 or more alcoholic drinks every day while using this product
  • ●Do not use

  • ●if you are allergic to acetaminophen or any of the inactive ingredients in this product
  • ●Ask a doctor before use if the user has liver disease.



  • ●Pain gets worse or lasts more than 5 days in children under 12 years
  • ●Fever gets worse or lasts more than 3 days
  • ●New symptoms occur
  • ●Redness or swelling is present
  • ●These could be signs of a serious condition.



OVERDOSAGE




DIRECTIONS











OTHER INFORMATION
  • ●Store at room temperature 15(59
  • ●Use by expiration date on package.

INACTIVE INGREDIENT





INACTIVE INGREDIENT

POVIDONE
STARCH, CORN

SODIUM STARCH GLYCOLATE TYPE A POTATO
STEARIC ACID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL SECTION














Acetaminophen



Acetaminophen



Acetaminophen

Acetaminophen TABLET

Product Information

Product Type Human prescription drug label Item Code (Source) NDC:24236-641(NDC:16103-0353)
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
ACETAMINOPHEN ACETAMINOPHEN 325 mg

Product Characteristics

Color Size Imprint Code Shape
white 5 mm PH020 ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:24236-641-02 30 in 1 BLISTER PACK

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075659 2011-03-09


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.