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

Warnings

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

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

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

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

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

Acetaminophen Extra Strength Caplets, 500 mg Carton

Acetaminophen Extra Strength Caplets, 500 mg Carton


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: 12/2009 Target Corporation