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

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PANADOL

GlaxoSmithKline Consumer Healtcare LP

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Acetaminophen 500 mg

Acetaminophen 500 mg

Pain reliever/fever reducer

  • •temporarily relieves minor aches and pains due to:
    • ∘headache
    • ∘backache
    • ∘muscular aches
    • ∘minor arthritis pain
  • •temporarily reduces fever

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

  • •pain gets worse or lasts more than 10 days
  • •fever gets worse or lasts more than 3 days
  • •redness or swelling is present
  • •any new symptoms appear

These could be signs of a serious condition.

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

Keep out of reach of children.

Overdose warning: Taking more than the recommended dose can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

  • do not take more than directed (see overdose warning)
  • •adults and children 12 years of age and over: take 2 caplets every 6 hours, while symptoms persist
  • •do not take more than 8 caplets in 24 hours, unless directed by a doctor
  • •children under 12 years of age: ask a doctor
  • do not take more than directed (see overdose warning)
  • •adults and children 12 years of age and over: take 2 tablets every 6 hours, while symptoms persist
  • •do not take more than 8 tablets in 24 hours, unless directed by a doctor
  • •children under 12 years of age: ask a doctor
  • •store below 30°C (86°F)

hypromellose, potassium sorbate, povidone, pregelatinized starch, starch, stearic acid, talc, triacetin

potassium sorbate, povidone, pregelatinized starch, starch, stearic acid, talc

1-800-981-3511 (English/Spanish) weekdays

Read and keep carton for complete information

Tamper Evident Feature: Do not use if printed bottle seal (under cap) is missing or broken.

Distributed by:

GlaxoSmithKline Consumer Healthcare, L.P.

Moon Township, PA 15108 U.S.A.

Principal Display Panel

NDC 0135-0136-04

PANADOL®

EXTRA STRENGTH

500

ACETAMINOPHEN

Pain Reliever

Fever Reducer

100 Caplets

©2011 GlaxoSmithKline

Made in China

101636XA

Principal Display Panel

NDC 0135-0135-04

PANADOL®

EXTRA STRENGTH

500

ACETAMINOPHEN

Pain Reliever

Fever Reducer

100 Tablets

©2011 GlaxoSmithKline

Made in India

101587XA

PANADOL

acetaminophen TABLET, FILM COATED

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0136
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
POTASSIUM SORBATE
POVIDONES
STARCH, CORN
STEARIC ACID
talc
triacetin

Product Characteristics

Color Size Imprint Code Shape
WHITE 18 mm PANADOL OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0136-09 2 in 1 PACKET
2 NDC:0135-0136-01 10 in 1 BOTTLE
3 NDC:0135-0136-02 24 in 1 BOTTLE
4 NDC:0135-0136-03 50 in 1 BOTTLE
5 NDC:0135-0136-04 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2011-03-18


PANADOL

acetaminophen TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:0135-0135
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
POTASSIUM SORBATE
POVIDONES
STARCH, CORN
STEARIC ACID
talc

Product Characteristics

Color Size Imprint Code Shape
WHITE 13 mm PANADOL ROUND

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:0135-0135-07 2 in 1 PACKET
2 NDC:0135-0135-01 10 in 1 BOTTLE
3 NDC:0135-0135-02 30 in 1 BOTTLE
4 NDC:0135-0135-03 60 in 1 BOTTLE
5 NDC:0135-0135-04 100 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part343 2011-03-18


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