PAIN RELIEVER- acetaminophen chewable gel

Pain Reliever by

Drug Labeling and Warnings

Pain Reliever by is a Otc medication manufactured, distributed, or labeled by Walgreens. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients (in each chewable gel)

Acetaminophen 500 mg

Purposes

Pain reliever/fever reducer

Uses

• temporarily relieves minor aches and pains due to
  • headache
  • the common cold 
  • backache
  • minor pain of arthritis
  • toothache
  • muscular arches
  • 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 the 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.

When using this product

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 (1-800-222-1222) right away: 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:

• chew 2 chewable gels every 6 hours while symptoms last
• do not take more than 6 chewable gels in 24 hours, unless directed by a doctor 
• do not take for more than 10 days unless directed by a doctor

• children under 12 years: do not use

Other information

• each gel contains: sodium 25 mg
• store at controlled room temperature 20-25ºC (68-77ºF)

Inactive ingredients

alcohol, ammonium glycyrrhizate, anhydrous citric acid, corn syrup, cyclohexane, D&C Red #33, ethylcellulose, glycerin, glycyrrhizin, malic acid, maltodextrin, natural and artificial type flavors,  pectin, polyethylene, propylene glycol, purified water, sucralose, sucrose, trisodium citrate dihydrate

Questions or comments?

Call1-877-753-3935 Monday-Friday 9AM-5PM EST

Principal display panel

Compare to the active ingredient in Tylenol® Extra Strength††

FOR ADULTS 

Pain Reliever

ACETAMINOPHEN 500 mg /

PAIN RELIEVER / FEVER REDUCER

Extra Strength 

Aspirin free & ibuprofen free

Cherry flavor

SOLID CHEWABLE GELS

††This product is not manufactured or distributed by Kenvue Brands LLC, distributor of Tylenol®Extra Strength.

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

DISTRIBUTED BY: WALGREEN CO.

DEERFIELD, IL 60015

Product Label

WALGREENS Pain Reliever

INGREDIENTS AND APPEARANCE

PAIN RELIEVER 
acetaminophen chewable gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-9235
Route of Administration	ORAL

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

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
ETHYLCELLULOSE (UNII: 7Z8S9VYZ4B)
AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCYRRHIZIN (UNII: 6FO62043WK)
MALIC ACID (UNII: 817L1N4CKP)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PECTIN (UNII: 89NA02M4RX)
POLYETHYLENE (UNII: UG00KM4WR7)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SUCROSE (UNII: C151H8M554)
CORN SYRUP (UNII: 9G5L16BK6N)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
CYCLOHEXANE (UNII: 48K5MKG32S)

Product Characteristics
Color	red	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	A
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-9235-05	50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/16/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M013	03/16/2026

Labeler - Walgreens (008965063)