PAIN RELIEVER- acetaminophen tablet 
L&R Distributors, 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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Select Brand 44-104

Active ingredient (in each tablet)

Acetaminophen 325 mg 

Purpose

Pain reliever/fever reducer 

Uses

Warnings

Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

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 the user has

liver disease.

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 in adults
  • new symptoms occur
  • pain gets worse or lasts more than 5 days in children under 12 years
  • fever gets worse or lasts more than 3 days
  • 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.

In case of accidental overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.  Prompt 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 tablets every 4 to 6 hours while symptoms last
  • do not take more than 10 tablets in 24 hours
  • do not take for more than 10 days unless directed by a doctor

children      6-11 years

  • take 1 tablet every 4 to 6 hours while symptoms last
  • do not take more than 5 tablets in 24 hours
  • do not take for more than 5 days unless directed by a doctor
children
under 6
years

 ask a doctor


Other information

Inactive ingredients

corn starch, povidone, sodium starch glycolate, stearic acid

Questions or comments?

1-800-426-9391 

Principal Display Panel

select brand®
the lower price name brand

NDC 15127-072-24

REGULAR STRENGTH/NON-ASPIRIN                 SAFETY SEALED
PAIN RELIEVER
ACETAMINOPHEN
PAIN RELIEVER/FEVER REDUCER

*Compare to the Active Ingredient of Regular Strength Tylenol®

325 mg Each

24 TABLETS

*This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Regular Strength Tylenol®.
50844    REV0615D10408

Distributed by:
SELECT BRAND® DISTRIBUTORS
Pine Bluff, AR 71603   USA
AC (870) 535-3635

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
Select Brand 44-104

Select Brand 44-104



PAIN RELIEVER 
acetaminophen tablet
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:15127-072
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg
Inactive Ingredients
Ingredient Name Strength
POVIDONES (UNII: FZ989GH94E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Color WHITE Score 2 pieces
Shape ROUND Size 10mm
Flavor Imprint Code 44;104
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:15127-072-08 1 in 1 CARTON
1 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
2 NDC:15127-072-24 1 in 1 CARTON
2 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part343 07/13/1990
Labeler - L&R Distributors, Inc. (012578514)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(15127-072)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(15127-072)

Revised: 2/2016
Document Id: 6a4022d4-89ef-43e5-b10b-9ee3b3508a69
Set id: ca7ae149-4c3f-449f-8536-c1135f04479a
Version: 15
Effective Time: 20160218
 
L&R Distributors, Inc.