TYLENOL EXTRA STRENGTH, TRAVEL BASIX- acetaminophen tablet, coated 
TYLENOL EXTRA STRENGTH, CVP HEALTH- acetaminophen tablet, coated 
TYLENOL EXTRA STRENGTH- acetaminophen tablet, coated 
Lil' Drug Store Products, Inc.

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Tylenol ® Extra Strength
Lil' Drug Store ®, TRAVEL BASIX, CVP ® HEALTH

Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

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

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 yearsask a doctor

Other information

Inactive ingredients

carnauba wax 1, corn starch 1, FD&C red no. 40 aluminum lake, hypromellose, magnesium stearate, modified starch 1, polyethylene glycol 1, powdered cellulose, pregelatinized starch, propylene glycol, shellac, sodium starch glycolate, titanium dioxide

1
contains one or more of these ingredients

Questions or comments?

call 1-877-895-3665 (toll-free) or 215-273-8755 (collect)

Product distributed by:
JOHNSON & JOHNSON CONSUMER INC.
McNeil Consumer Healthcare Division
Fort Washington, PA 19034 USA

Repackaged and distributed by:
Lil' Drug Store Products, Inc., 9300 Earhart Lane SW
Cedar Rapids, IA 52404

Tylenol ES Caplets, Lil' Drug Store ® - PDP/Package

TYLENOL ®

FOR ADULTS

Acetaminophen

Pain Reliever

Fever Reducer

EXTRA STRENGTH

500 mg each

6

Caplets

Lil'

Drug Store ®

Principal Display Panel - 500 mg Caplet Pouch Carton

Tylenol ES Caplets, TRAVEL BASIX - PDP/Package

TYLENOL ®

FOR ADULTS

Acetaminophen Pain Reliever Fever Reducer

Extra Strength

[caplets image]

500 mg each

4

Caplets

2 POUCHES OF 2 CAPLETS EACH

[TRAVEL BASIX logo]

PDP/Package

Tylenol ES Caplets, CVP ® HEALTH - PDP/Package

TYLENOL ®

FOR ADULTS

Acetaminophen Pain Reliever Fever Reducer

Extra Strength

[caplets image]

500 mg each

4

Caplets

2 POUCHES OF 2 CAPLETS EACH

[CVP ® HEALTH logo]

PDP/Package

Tylenol ® ES Caplets, Lil' Drug Store ® 25ct Unit Dose Box - PDP/Package

TYLENOL®

FOR ADULTS

Acetaminophen

Pain Reliever

Fever Reducer

Extra Strength

[caplets image]

25 Pouches of 2 Caplets each - 500 mg each

[Lil' Drug Store logo]

PDP/Package

Tylenol ® ES Caplets, Lil' Drug ® Store 30ct Unit Dose Box - PDP/Package

TYLENOL®

FOR ADULTS

Acetaminophen

Pain Reliever

Fever Reducer

Extra Strength

[caplets image]

30 Pouches of 2 Caplets each - 500 mg each

[Lil' Drug Store logo]

PDP/Package

TYLENOL EXTRA STRENGTH, TRAVEL BASIX 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6447
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)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize18mm
FlavorImprint Code TYLENOL;500
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-6447-22 in 1 CARTON11/29/2022
12 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01311/22/2022
TYLENOL EXTRA STRENGTH, CVP HEALTH 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6547
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
STARCH, CORN (UNII: O8232NY3SJ)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize18mm
FlavorImprint Code TYLENOL;500
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-6547-22 in 1 CARTON05/06/2022
12 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01305/06/2022
TYLENOL EXTRA STRENGTH 
acetaminophen tablet, coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-9747
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)  
STARCH, CORN (UNII: O8232NY3SJ)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SHELLAC (UNII: 46N107B71O)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
Product Characteristics
ColorwhiteScoreno score
ShapeOVALSize18mm
FlavorImprint Code TYLENOL;500
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:66715-9747-11 in 1 CARTON04/16/201806/29/2024
12 in 1 POUCH; Type 0: Not a Combination Product
2NDC:66715-9747-22 in 1 CARTON04/13/2019
22 in 1 POUCH; Type 0: Not a Combination Product
3NDC:66715-9747-33 in 1 CARTON06/29/2018
32 in 1 POUCH; Type 0: Not a Combination Product
4NDC:66715-9747-730 in 1 CARTON04/09/2018
42 in 1 POUCH; Type 0: Not a Combination Product
5NDC:66715-9747-825 in 1 BOX, UNIT-DOSE04/19/2022
52 in 1 POUCH; Type 0: Not a Combination Product
6NDC:66715-9747-930 in 1 BOX, UNIT-DOSE04/19/2022
62 in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01308/09/2011
Labeler - Lil' Drug Store Products, Inc. (093103646)

Revised: 1/2024
Document Id: 0f53ea26-7ef3-62b0-e063-6394a90addb4
Set id: fa951d50-b79c-4161-8c81-fcf386b0964e
Version: 10
Effective Time: 20240119
 
Lil' Drug Store Products, Inc.