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

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:

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 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

Other information

Inactive Ingredients

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

Questions or comments?

1-800-426-9391

Principal Display Panel

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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 Type HUMAN OTC DRUG Item Code (Source) NDC:15127-735
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
HYPROMELLOSES (UNII: 3NXW29V3WO)  
POVIDONE (UNII: FZ989GH94E)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
CASTOR OIL (UNII: D5340Y2I9G)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
Color WHITE Score no score
Shape OVAL (Tablet) Size 17mm
Flavor Imprint Code 44;175
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:15127-735-19 2 in 1 CARTON 04/02/1993
1 4 in 1 BLISTER PACK; Type 0: Not a Combination Product
2 NDC:15127-735-09 1 in 1 CARTON 04/02/1993
2 24 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
3 NDC:15127-735-16 1 in 1 CARTON 04/02/1993
3 50 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
4 NDC:15127-735-08 1 in 1 CARTON 04/02/1993
4 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
5 NDC:15127-735-05 500 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/02/1993
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH NOT FINAL part343 04/02/1993
Labeler - L&R Distributors, Inc. (012578514)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 832867894 MANUFACTURE(15127-735)
Establishment
Name Address ID/FEI Business Operations
LNK International, Inc. 038154464 PACK(15127-735)

Revised: 5/2017
Document Id: b69d071f-dfea-4702-a67a-a570cc48f766
Set id: e22f4952-5b2d-b2bd-6d38-4353f77420b0
Version: 9
Effective Time: 20170505
 
L&R Distributors, Inc.