PAIN RELIEF- acetaminophen capsule, liquid filled 
Meijer Distribution 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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Meijer Distribution, Inc. Pain Relief Drug Facts

Active ingredient (in each capsule)

Acetaminophen 325 mg

Purpose

Pain reliever/fever reducer

Uses

•
temporarily relieves minor aches and pains due to:
•
headache
•
muscular aches
•
backache
•
minor pain of arthritis
•
the common cold
•
toothache
•
premenstrual and menstrual cramps
•
temporarily reduces fever

Warnings

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

•
adult takes more than 4,000 mg of acetaminophen 24 hours
•
child takes more than 5 doses in 24 hours
•
taken with other drugs containing acetaminophen
•
adult has 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 the user

•
has liver disease
•
is a child with pain of arthritis

Ask a doctor or pharmacist before use if the user is

taking the blood thinning drug warfarin

Stop use and ask a doctor if

•
pain gets worse or lasts more than 10 days (for adults) or 5 days (for children)
•
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 capsules every 4 to 6 hours while symptoms last
•
do not take more than 10 capsules in 24 hours
•
do not use for more than 10 days unless directed by a doctor

children 6-11 years
•
take 1 capsule every 4 to 6 hours while symptoms last
•
do not take more than 5 capsules in 24 hours
•
do not use for more than 5 days unless directed by a doctor

children under

6 years

ask a doctor

Other information

•
store at 20-25°C (68-77°F)

Inactive ingredients

edible ink*, FD&C red no. 40, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitol sorbitan solution *may contain this ingredient

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

Compare to Tylenol® Liquid Gels active ingredient

REGULAR STRENGTH

pain relief 325 mg Each

Acetaminophen | Pain Reliever | Fever Reducer

90 Liquid Gels**

**Liquid-Filled Capsules

actual size

6g2-6e-pain-relief-1.jpg
6g2-6e-pain-relief-2.jpg
PAIN RELIEF 
acetaminophen capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-104
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN325 mg
Inactive Ingredients
Ingredient NameStrength
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorBROWNScoreno score
ShapeOVALSize16mm
FlavorImprint Code A325
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:41250-104-751 in 1 CARTON05/04/201602/29/2020
190 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34305/04/201602/29/2020
Labeler - Meijer Distribution Inc (006959555)

Revised: 12/2020
Document Id: d9aedce2-e908-4bdb-b21b-e54037317acf
Set id: 265beead-fa18-4ae7-8336-cb8ca63e36a3
Version: 4
Effective Time: 20201230
 
Meijer Distribution Inc