CIRCLE K PAIN RELIEVER EXTRA STRENGTH- acetaminophen tablet 
CIRCLE K PAIN RELIEVER- acetaminophen tablet 
Lil' Drug Store Products, Inc

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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Circle K™ Pain Reliever

Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

  • temporarily relieves minor aches and pains due to:
    • headache
  • the common cold
    • 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 are allergic to acetaminophen or any of the inactive ingredients in this product

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.

Overdose warning

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
    • do not take for more than 10 days unless directed by a doctor
  • children under 12 years: do not use

Other information

  • store between 68-77°F (20-25°C)

Inactive ingredients

corn starch, croscarmellose sodium1, hypromellose1, lactose monohydrate1, magnesium stearate1, maltodextrin1, medium-chain triglycerides1, mineral oil1, polydextrose1, polyethylene glycol1, polyvinyl alcohol1, povidone, purified water1, sodium starch glycolate1, stearic acid1, talc1, titanium dioxide

1
contains one or more of these ingredients

Questions or comments?

Call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

Proudly distributed by Circle K Stores Inc.

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5837

Compare to the Active Ingredient
in Tylenol® Extra Strength**

CIRCLE K™

Pain Reliever

Acetaminophen
Pain Reliever/Fever Reducer, 500 mg

Extra
Strength

ACTUAL SIZE

24 Caplets

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5837

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5737

Compare to the Active Ingredient
in Tylenol® Extra Strength**

K®

Pain Reliever

Acetaminophen
Pain Reliever/Fever Reducer 500 mg

Extra
Strength

ACTUAL SIZE

24 Caplets

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5737

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5637

Compare to the Active Ingredient
in Tylenol® Extra Strength**

K®

Pain Reliever

Acetaminophen
Pain Reliever/Fever Reducer 500 mg

Extra
Strength

ACTUAL SIZE

24 Caplets

PRINCIPAL DISPLAY PANEL - 24 Tablet Bottle Carton - 66715-5637
CIRCLE K PAIN RELIEVER  EXTRA STRENGTH
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5837
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
Inactive Ingredients
Ingredient NameStrength
Starch, Corn (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Lactose Monohydrate (UNII: EWQ57Q8I5X)  
Magnesium Stearate (UNII: 70097M6I30)  
Maltodextrin (UNII: 7CVR7L4A2D)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
Mineral Oil (UNII: T5L8T28FGP)  
Polydextrose (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (94000 MW) (UNII: C1MS7RRZ6L)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Water (UNII: 059QF0KO0R)  
Sodium Starch Glycolate Type A Corn (UNII: AG9B65PV6B)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Talc (UNII: 7SEV7J4R1U)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize18mm
FlavorImprint Code P500
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-5837-41 in 1 CARTON08/04/201610/17/2022
124 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34311/01/201410/17/2022
CIRCLE K PAIN RELIEVER 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5737
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
Inactive Ingredients
Ingredient NameStrength
Starch, Corn (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Maltodextrin (UNII: 7CVR7L4A2D)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
Mineral Oil (UNII: T5L8T28FGP)  
Polydextrose (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (94000 MW) (UNII: C1MS7RRZ6L)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Water (UNII: 059QF0KO0R)  
Sodium Starch Glycolate Type A Corn (UNII: AG9B65PV6B)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Talc (UNII: 7SEV7J4R1U)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize18mm
FlavorImprint Code TCL341
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-5737-41 in 1 CARTON08/04/201610/17/2022
124 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34311/01/201410/17/2022
CIRCLE K PAIN RELIEVER 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-5637
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen500 mg
Inactive Ingredients
Ingredient NameStrength
Starch, Corn (UNII: O8232NY3SJ)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
Maltodextrin (UNII: 7CVR7L4A2D)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
Mineral Oil (UNII: T5L8T28FGP)  
Polydextrose (UNII: VH2XOU12IE)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POLYVINYL ALCOHOL (94000 MW) (UNII: C1MS7RRZ6L)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
Water (UNII: 059QF0KO0R)  
Sodium Starch Glycolate Type A Corn (UNII: AG9B65PV6B)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Talc (UNII: 7SEV7J4R1U)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVALSize18mm
FlavorImprint Code AV;0821
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-5637-41 in 1 CARTON08/04/201610/17/2022
124 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34311/01/201410/17/2022
Labeler - Lil' Drug Store Products, Inc (093103646)

Revised: 10/2020
Document Id: 3922e493-940d-4619-801e-e96d4598eee6
Set id: 441fd449-31b3-4f34-a0f2-a8979c2e80f7
Version: 4
Effective Time: 20201005
 
Lil' Drug Store Products, Inc