DrugCite

EXTRA STRENGTH NON ASPIRIN PAIN RELIEF - acetaminophen tablet 
Stephen L. LaFrance Pharmacy, Inc.

Select Brand 44-531

Active ingredient (n each tablet)

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 8 tablets in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks every day while using this product

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. 

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: Taking more than the recommended dose (overdose) may cause liver damage.  In case of overdose, get medical help or contact a Poison Control Center right away.  Quick medical attention is critical for adults as well as for children even if you do not notice any signs of symptoms. 

Directions

  • do not take more than directed (see overdose warning)
  • adults and children 12 years and over
    • take 2 tablets every 4 to 6 hours while symptoms last
    • do not take more than 8 tablets in 24 hours
    • do not take for more than 10 days unless directed by a doctor
  • children under 12 years: do not use this adult extra strength product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage

Other information

  • store at controlled room temperature 15º-30ºC (59º-86ºF)
  • see end flap for expiration date and lot number 

Inactive ingredients

D&C yellow #10 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, polyethylene glycol, polyvinyl alcohol, povidone, sodium starch glycolate*, starch, stearic acid, sucralose, talc, titanium dioxide

*may contain this ingredient 

Principal display panel

SEE NEW WARNINGS INFORMATION

select brand®

the lower price name brand

NDC 15127-972-24

EXTRA STRENGTH/NON-ASPIRIN

PAIN RELIEVER

ACETAMINOPHEN

Easy to Swallow Sweet Coated

PAIN RELIEVER/FEVER REDUCER • NON-ASPIRIN

†Compare to the Active Ingredient of Tylenol® Extra Strength EZ Tabs

EASY TABS 500 mg Each

24 TABLETS

†This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Tylenol® Extra Strength EZ Tabs.

50844    REV1010B53108

Distributed by:

SELECT BRAND® DISTRIBUTOR

Pine Bluff, AR 71603

AC (870) 535-3635

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

Select Brand 44-531

Select Brand 44-531


EXTRA STRENGTH NON ASPIRIN PAIN RELIEF 
acetaminophen  tablet
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 15127-972
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 500 mg
Inactive Ingredients
Ingredient Name Strength
D&C YELLOW NO. 10  
FD&C YELLOW NO. 6  
FD&C RED NO. 40  
STARCH, CORN  
TALC  
TITANIUM DIOXIDE  
POLYVINYL ALCOHOL  
Product Characteristics
Color RED Score no score
Shape ROUND Size 11mm
Flavor Imprint Code 44;531
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 15127-972-08 1 BOTTLE In 1 CARTON contains a BOTTLE
1 24 TABLET In 1 BOTTLE This package is contained within the CARTON (15127-972-08)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part343 12/11/2022

Labeler - Stephen L. LaFrance Pharmacy, Inc. (043562370)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 038154464 PACK
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 832867894 MANUFACTURE
Revised: 08/2012Stephen L. LaFrance Pharmacy, Inc.