GOOD SENSE PAIN RELIEF- acetaminophen tablet 
L. Perrigo Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Perrigo Pain Relief Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

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

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 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.

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 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

Other information

store at 20-25ºC (68-77ºF)

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 ingredients

Questions or comments?

1-800-719-9260

Principal Display Panel

GOODSENSE®

Extra Strength

Pain Relief Caplets

Pain Reliever/Fever Reducer

Acetaminophen

For Adults

Actual Size

250 Caplets – 500 mg Each

Compare to active ingredient of Extra Strength Tylenol®

484-c2-pain-relief
GOOD SENSE PAIN RELIEF 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-0484
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
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
ColorWHITEScoreno score
ShapeOVALSize16mm
FlavorImprint Code L484
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0113-0484-5210 in 1 VIAL; Type 0: Not a Combination Product09/15/198912/01/2021
2NDC:0113-0484-621 in 1 CARTON09/15/1989
224 in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:0113-0484-711 in 1 CARTON09/15/1989
350 in 1 BOTTLE; Type 0: Not a Combination Product
4NDC:0113-0484-781 in 1 CARTON09/15/1989
4100 in 1 BOTTLE; Type 0: Not a Combination Product
5NDC:0113-0484-761 in 1 CARTON09/15/198909/30/2019
5120 in 1 BOTTLE; Type 0: Not a Combination Product
6NDC:0113-0484-90500 in 1 BOTTLE; Type 0: Not a Combination Product09/15/1989
7NDC:0113-0484-822 in 1 CARTON09/15/1989
7100 in 1 BOTTLE; Type 0: Not a Combination Product
8NDC:0113-0484-02550 in 1 BOTTLE; Type 0: Not a Combination Product09/15/198902/29/2020
9NDC:0113-0484-851 in 1 CARTON03/23/2022
9250 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34309/15/1989
Labeler - L. Perrigo Company (006013346)

Revised: 3/2022
Document Id: 7688cfd4-2efa-4a56-8443-591e36ebc809
Set id: 7f78028a-484b-48b3-a37a-1e0b055bbefc
Version: 9
Effective Time: 20220323
 
L. Perrigo Company