DailyMed - GOOD SENSE PAIN RELIEF- acetaminophen tablet

NDC Code(s): 0113-0484-02, 0113-0484-52, 0113-0484-62, 0113-0484-71, view more
0113-0484-76, 0113-0484-78, 0113-0484-82, 0113-0484-85, 0113-0484-90
Packager: L. Perrigo Company

Category: HUMAN OTC DRUG LABEL
DEA Schedule: None

Drug Label Information

Updated January 9, 2025

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Active ingredient (in each caplet)
Acetaminophen 500 mg

Acetaminophen 500 mg
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Purpose
Pain reliever/fever reducer

Pain reliever/fever reducer
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Uses
• temporarily relieves minor aches and pains due to: • the common cold - • headache - • backache - • minor pain of arthritis - • toothache - • muscular aches - • premenstrual and menstrual ...

•

temporarily relieves minor aches and pains due to:

•

the common cold

•

headache

•

backache

•

minor pain of arthritis

•

toothache

•

muscular aches

•

premenstrual and menstrual cramps

•

temporarily reduces fever

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Warnings
Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take - • more than 4,000 mg of acetaminophen in 24 hours - • with other drugs containing acetaminophen - • 3 or ...

Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take

•

more than 4,000 mg of acetaminophen in 24 hours

•

with other drugs containing acetaminophen

•

3 or more alcoholic drinks every day while using this product

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

•

skin reddening

•

blisters

•

rash

If a skin reaction occurs, stop use and seek medical help right away.

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.

•

if you have ever had an allergic reaction to this product or any of its ingredients

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

•

new symptoms occur

•

redness or swelling is present

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.

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

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Directions

• do not take more than directed (see overdose warning) adults and children 12 years and over - • take 2 caplets every 6 hours while symptoms last - • do not take more than 6 caplets in ...

Other information
• store at 20-25ºC (68-77ºF)

•

store at 20-25ºC (68-77ºF)

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Inactive ingredients
carnauba wax, corn starch*, croscarmellose sodium*, hypromellose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate*, stearic acid - *may contain one or more of these ...

carnauba wax, corn starch*, croscarmellose sodium*, hypromellose, polyethylene glycol, povidone, pregelatinized starch, sodium starch glycolate*, stearic acid

*may contain one or more of these ingredients
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Questions or comments?
1-800-719-9260

1-800-719-9260
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Principal Display Panel
GOODSENSE® Extra Strength - Pain Relief Caplets - Pain Reliever/Fever Reducer - Acetaminophen - For Adults - Actual Size - 24 Caplets -500 mg Each - Compare to active ingredient of Extra Strength ...

GOODSENSE®

Extra Strength

Pain Relief Caplets

Pain Reliever/Fever Reducer

Acetaminophen

For Adults

Actual Size

24 Caplets -500 mg Each

Compare to active ingredient of Extra Strength Tylenol®

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INGREDIENTS AND APPEARANCE

Product Information

GOOD SENSE PAIN RELIEF acetaminophen tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:0113-0484
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg

Ingredient Name	Strength
Inactive Ingredients
CARNAUBA WAX (UNII: R12CBM0EIZ)
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
STEARIC ACID (UNII: 4ELV7Z65AP)
STARCH, CORN (UNII: O8232NY3SJ)
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)

Product Characteristics
Color	WHITE	Score	no score
Shape	OVAL	Size	16mm
Flavor		Imprint Code	L484
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:0113-0484-52	10 in 1 VIAL; Type 0: Not a Combination Product	09/15/1989	12/01/2021
2	NDC:0113-0484-62	1 in 1 CARTON	09/15/1989
2		24 in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC:0113-0484-71	1 in 1 CARTON	09/15/1989
3		50 in 1 BOTTLE; Type 0: Not a Combination Product
4	NDC:0113-0484-78	1 in 1 CARTON	09/15/1989
4		100 in 1 BOTTLE; Type 0: Not a Combination Product
5	NDC:0113-0484-76	1 in 1 CARTON	09/15/1989	09/30/2019
5		120 in 1 BOTTLE; Type 0: Not a Combination Product
6	NDC:0113-0484-90	500 in 1 BOTTLE; Type 0: Not a Combination Product	09/15/1989
7	NDC:0113-0484-82	2 in 1 CARTON	09/15/1989	03/26/2016
7		100 in 1 BOTTLE; Type 0: Not a Combination Product
8	NDC:0113-0484-02	550 in 1 BOTTLE; Type 0: Not a Combination Product	09/15/1989	02/29/2020
9	NDC:0113-0484-85	1 in 1 CARTON	03/23/2022	03/31/2025
9		250 in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC Monograph Drug	M013	09/15/1989

Labeler - L. Perrigo Company (006013346)

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Published Date (What is this?)	Version	Files
Jan 13, 2025	10 (current)	download
Mar 24, 2022	9	download
Dec 8, 2021	8	download
Dec 13, 2019	7	download
Dec 19, 2017	6	download
Nov 28, 2014	5	download
Nov 18, 2013	4	download
Sep 11, 2012	3	download
Jun 29, 2012	2	download
Apr 28, 2011	1	download

	RxCUI	RxNorm NAME	RxTTY
1	198440	acetaminophen 500 MG Oral Tablet	PSN
2	198440	acetaminophen 500 MG Oral Tablet	SCD
3	198440	APAP 500 MG Oral Tablet	SY

Label: GOOD SENSE PAIN RELIEF- acetaminophen tablet

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Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

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

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

adults and children 12 years and over	• take 2 caplets every 6 hours while symptoms last • do not take more than 6 caplets in 24 hours, unless directed by a doctor • do not use for more than 10 days unless directed by a doctor
children under 12 years	ask a doctor

	NDC
1	0113-0484-02
2	0113-0484-52
3	0113-0484-62
4	0113-0484-71
5	0113-0484-76
6	0113-0484-78
7	0113-0484-82
8	0113-0484-85
9	0113-0484-90

Label: GOOD SENSE PAIN RELIEF- acetaminophen tablet

View Package Photos

Drug Label Info

Safety

Related Resources

More Info For This Drug

Drug Label Information

Do not use

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

If pregnant or breast-feeding,

Keep out of reach of children.

Find additional resources

Safety

Related Resources

More Info on this Drug

GOOD SENSE PAIN RELIEF- acetaminophen tablet

Number of versions: 10

GOOD SENSE PAIN RELIEF- acetaminophen tablet

GOOD SENSE PAIN RELIEF- acetaminophen tablet

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GOOD SENSE PAIN RELIEF- acetaminophen tablet

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