PAIN RELIEF ACETAMINOPHEN EXTRA STRENGTH- acetaminophen tablet, coated 
Rite Aid Corporation

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Rite Aid 44-519

Active ingredient (in each gelcap)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

Warnings

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

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

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

Do not use

  • if you are allergic to acetaminophen or any of the inactive ingredients in this product
  • 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
  • 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. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Other information

Inactive ingredients

croscarmellose sodium, D&C red #33, FD&C blue #1, FD&C red #40, gelatin, hydroxypropyl cellulose, hypromellose, iron oxide black, iron oxide red, iron oxide yellow, polyethylene glycol, povidone, pregelatinized starch, propylene glycol, shellac glaze, stearic acid, titanium dioxide

Questions or comments?

 1-800-426-9391

Principal Display Panel

NDC 11822-0519-5

Compare to the active ingredient in
Extra Strength Tylenol® Rapid Release Gels*

EXTRA STRENGTH PAIN RELIEF
ACETAMINOPHEN

ACETAMINOPHEN 500 mg
PAIN RELIEVER/FEVER REDUCER

contains no aspirin

ACTUAL SIZE

50
GELCAPS

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY
SEAL UNDER CAP IS BROKEN OR MISSING

*This product is not manufactured or distributed by Johnson
& Johnson Corporation, owner of the registered trademark
Extra Strength Tylenol® Rapid Release Gels.
50844        REV0322G51915

DISTRIBUTED BY: RITE AID
30 HUNTER LANE,
CAMP HILL, PA 17011
www.riteaid.com

SATISFACTION
GUARANTEE
If you're not satisfied, we'll
happily refund your money.

Rite Aid 44-519

Rite Aid 44-519

PAIN RELIEF ACETAMINOPHEN  EXTRA STRENGTH
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-0519
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
Colorred, blueScoreno score
ShapeOVALSize19mm
FlavorImprint Code L;5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-0519-81 in 1 CARTON05/10/2004
124 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2NDC:11822-0519-51 in 1 CARTON05/10/2004
250 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:11822-0519-21 in 1 CARTON05/10/2004
3100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:11822-0519-9150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/10/2004
5NDC:11822-0519-3225 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/10/2004
6NDC:11822-0519-11 in 1 CARTON05/10/200401/08/2022
62 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01305/10/2004
Labeler - Rite Aid Corporation (014578892)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464manufacture(11822-0519) , pack(11822-0519)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837manufacture(11822-0519)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(11822-0519)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088manufacture(11822-0519)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(11822-0519)

Revised: 6/2023
Document Id: 97b0b668-f83b-4bf6-b7d2-1de2386f66e2
Set id: 26c0641e-1cdd-4084-939d-01dbd36ab9b7
Version: 21
Effective Time: 20230617
 
Rite Aid Corporation