ACETAMINOPHEN - acetaminophen tablet 
Stephen L. LaFrance Pharmacy, Inc.

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Pain Reliever

Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

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

Warning

Liver warning:

This product contains acetaminophen. Severe liver damage may occur if you take:

• more then 8 caplets 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 or symptoms.

Directions

• do not take more than directed

(see overdose warning)

• adults and children 12 years and over
• take 2 caplets every 4 to 6 hours while symptoms last
• do not take more than 8 caplets 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 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

*may contain this ingredient

Questions or comments?

1-800-426-9391

PRODUCT PACKAGING

The product packaging shown below represents a sample of that currenly in use. Additional packaging may also be available.

select brand®

the lower price name brand

EXTRA STRENGTH/NON-ASPRIN

PAIN RELIEVER

NDC 15127-735-08

SEE NEW WARNINGS

SAFETY SEALED

PAIN RELIEVER/FEVER REDUCER

NON-ASPRIN ACETAMINOPHEN

†Compare to the active Ingredient of Extra Strength Tylenol®

500 mg EACH

100 CAPLETS

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

50844         ORG070917512

Distributed by:

SELECT BRAND® DISTRIBUTORS

Pine Bluff, AR 71603 USA

AC (870) 535-3635

ACETAMINOPHEN  acetaminophen   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 15127-175 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 Hypromellose   Povidone   Stearic Acid   Castor Oil   Sodium Starch Glycolate Type A Potato

Product Characteristics Color WHITE Score no score Shape CAPSULE (Tablet) Size 18mm Flavor Imprint Code 44;175 Contains

Packaging # NDC Package Description Multilevel Packaging 1 15127-175-08 1 BOTTLE In 1 CARTON contains a BOTTLE, PLASTIC 1 24 TABLET In 1 BOTTLE, PLASTIC This package is contained within the CARTON (15127-175-08) 2 15127-175-15 1 BOTTLE In 1 CARTON contains a BOTTLE, PLASTIC 2 50 TABLET In 1 BOTTLE, PLASTIC This package is contained within the CARTON (15127-175-15) 3 15127-175-12 1 BOTTLE In 1 CARTON contains a BOTTLE, PLASTIC 3 100 TABLET In 1 BOTTLE, PLASTIC This package is contained within the CARTON (15127-175-12) 4 15127-175-14 500 TABLET In 1 BOTTLE, PLASTIC None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	04/02/1993

Labeler - Stephen L. LaFrance Pharmacy, Inc. (043562370)

Registrant - L.N.K. International, Inc. (832867837)

Establishment
Name	Address	ID/FEI	Operations
L.N.K. International, Inc		832867894	MANUFACTURE

Revised: 08/2010Stephen L. LaFrance Pharmacy, Inc.