UP AND UP ACETAMINOPHEN EXTRA STRENGTH - acetaminophen tablet 
Target Corporation

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Target Corporation Acetaminophen Extra Strength Caplets, 500 mg Drug Facts

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain reliever/fever reducer

Uses

• temporarily relieves minor aches and pains due to:
• the common cold
• headache
• 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 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.

In case of overdose, get medical help or contact a Poison Control Center right away. (1-800-222-1222) 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 Liver warning)

adults and children 12 years and over	take 2 caplets every 6 hours while symptoms last do not take more than 8 caplets in 24 hours
children under 12 years	do not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Other information

• store at 20º-25ºC (68º-77ºF)

Inactive ingredients

carnauba wax*, croscarmellose sodium*, hypromellose, polyethylene glycol, povidone, sodium metabisulfite*, sodium starch glycolate*, starch, stearic acid *may contain one or more of these ingredients

Questions?

Call 1-800-910-6874

Principal Display Panel

Acetaminophen Extra Strength Caplets, 500 mg

Compare to active ingredient in Extra Strength Tylenol®

See New Warnings Information

Pain Reliever/Fever Reducer

# Caplets {Replace "#" with the number of caplets in the package}

Shown Actual Size Above

UP AND UP ACETAMINOPHEN  EXTRA STRENGTH acetaminophen   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 11673-484 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 CARNAUBA WAX   CROSCARMELLOSE SODIUM   HYPROMELLOSES   POLYETHYLENE GLYCOL   POVIDONE   SODIUM METABISULFITE   STEARIC ACID

Product Characteristics Color WHITE Score no score Shape CAPSULE (caplet) Size 16mm Flavor Imprint Code L484 Contains

Packaging # NDC Package Description Multilevel Packaging 1 11673-484-71 1 BOTTLE In 1 CARTON contains a BOTTLE 1 50 TABLET In 1 BOTTLE This package is contained within the CARTON (11673-484-71) 2 11673-484-78 1 BOTTLE In 1 CARTON contains a BOTTLE 2 100 TABLET In 1 BOTTLE This package is contained within the CARTON (11673-484-78) 3 11673-484-85 1 BOTTLE In 1 CARTON contains a BOTTLE 3 250 TABLET In 1 BOTTLE This package is contained within the CARTON (11673-484-85) 4 11673-484-90 500 TABLET In 1 BOTTLE None 5 11673-484-01 1 BOTTLE In 1 CARTON contains a BOTTLE 5 100 TABLET In 1 BOTTLE This package is contained within the CARTON (11673-484-01) and contains a CARTON 5 1 VIAL In 1 CARTON This package is contained within the BOTTLE and contains a VIAL (11673-484-52) 5 11673-484-52 10 TABLET In 1 VIAL This package is contained within a CARTON and a BOTTLE and a CARTON (11673-484-01)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part343	12/02/2009

Labeler - Target Corporation (006961700)

Revised: 12/2009Target Corporation