PAIN RELIEVER- acetaminophen tablet, film coated 
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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Pain Reliever

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

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

Warnings

Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 6 caplets (3,000 mg) in 24 hours. 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.

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

  • do not take more than directed
  • 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 take for more than 10 days unless directed by a doctor
  • children under 12 years: ask a doctor

Other information

  • store at 25ºC (77ºF); excursions permitted between 15°-30°C (59°-86°F)
  • see end flap for expiration date and lot number

Inactive Ingredients

caster oil, hypromellose, povidone, sodium starch glycolate, starch, stearic acid

Questions or comments?

1-800-426-9391

Principal Display Panel

select brand®
the lower price name brand

NDC 15127-735-16

EXTRA STRENGTH/NON-ASPIRIN

PAIN RELIEVER

ACETAMINOPHEN PAIN RELIEVER/FEVER REDUCER

*Compare to the Active Ingredient of Extra Strength Tylenol® Caplets

50 CAPLETS       500 mg EACH

*This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Extra Strength Tylenol® Caplets.
50844         REV0715B17515

SATISFACTION
GUARANTEED
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brand®

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

Select Brand 44-175

Select Brand 44-175

PAIN RELIEVER 
acetaminophen tablet, film coated
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:15127-735
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POVIDONE (UNII: FZ989GH94E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CASTOR OIL (UNII: D5340Y2I9G)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
ColorWHITEScoreno score
ShapeOVAL (Tablet) Size17mm
FlavorImprint Code 44;175
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:15127-735-192 in 1 CARTON04/02/199308/03/2021
14 in 1 BLISTER PACK; Type 0: Not a Combination Product
2NDC:15127-735-091 in 1 CARTON04/02/199308/03/2021
224 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3NDC:15127-735-161 in 1 CARTON04/02/199308/03/2021
350 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4NDC:15127-735-081 in 1 CARTON04/02/199308/03/2021
4100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5NDC:15127-735-05500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/02/199308/03/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34304/02/199308/03/2021
Labeler - L&R Distributors, Inc. (012578514)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464PACK(15127-735)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305PACK(15127-735)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.868734088PACK(15127-735)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837MANUFACTURE(15127-735) , PACK(15127-735)

Revised: 5/2019
 
L&R Distributors, Inc.