ACETAMINOPHEN- acetaminophen tablet 
Cardinal Health

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Acetaminophen 500 mg Caplets

Drug Information

Acetaminophen

500 mg Caplets

Extra Strength

Pain Reliever/Fever Reducer

Contains No Aspirin

TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING

Active ingredient (in each caplet)

Acetaminophen 500 mg

Purpose

Pain Reliever/Fever Reducer

Keep Out of Reach of Children

Keep out of reach of children.

Uses

temporarily relieves minor aches and pains due to:

headache
muscular aches
backache
minor pain of arthritis
the common cold
toothache
premenstrual and menstrual cramps
temporarily reduces fever

Warnings

Alcohol warning: If you consume 3 or more alcoholic drinks every day, ask your doctor whether you should take acetaminophen or other pain relievers or fever reducers. Acetaminophen may cause liver damage.

Do not use with any other product containing acetaminophen

Stop use and ask a doctor if

pain gets worse or lasts for more than 10 days
fever gets worse or lasts for 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.

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 (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 overdose warning)
Adults and children 12 years of age 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 use for more than 10 days unless directed by a doctor
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.

Inactive ingredients

pregelatinized starch, povidone, stearic acid, hypromellose, polyethylene glycol, titanium dioxide, carnauba wax

How Supplied

How Supplied

Acetaminophen Extra Strength Caplets are available as follows:

500 mg - White to off-white, capsule shaped, film coated caplets with 112 debossed on one side.

NDC 51079-396-20 - Unit dose blister packages of 100 (10 cards of 10 caplets each).

NDC 51079-396-19 - Robot Ready blister packages of 25 (25 cards of 1 caplet each).

Storage

Store between 20-25°C (68-77°F)

Other Information

do not use if blister units are torn, broken or show any signs of tampering

Questions? 1-800-848-0462

Serious side effects associated with use of this product may be reported to this number.

Manufactured by:

Amneal Pharmaceuticals Corp.

Paterson, NJ 07504

Packaged and Distributed by:

UDL Laboratories, Inc.

Rockford, IL 61103

S-8777 R3

1/09

Principal Display Panel

Acetaminophen Caplets

500 mg

Extra Strength

10 Caplets

Bag Label
ACETAMINOPHEN 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-5552(NDC:51079-396)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
Product Characteristics
ColorWHITEScoreno score
ShapeCAPSULESize10mm
FlavorImprint Code 112
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55154-5552-010 in 1 BAG06/02/201101/31/2012
11 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Unapproved drug other06/02/201101/31/2012
Labeler - Cardinal Health (188557102)
Establishment
NameAddressID/FEIBusiness Operations
Cardinal Health188557102REPACK(55154-5552)

Revised: 4/2018
 
Cardinal Health