DrugCite

ACETAMINOPHEN - acetaminophen tablet 
NASH-FINCH COMPANY

Our Family 44-104

Active ingredient (in each tablet)

Acetaminophen 325 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

Warnings

Liver Warning:

This product contains acetaminophen.  Severe liver damage may occur if:
  • adults take more than 12 tablets in 24 hours, which is the maximum daily amount
  • child takes more than 5 doses in 24 hours
  • taken with other drugs containing acetaminophen
  • adult has 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 the user has

  • liver disease

Ask a doctor or pharmacist before use if the user is

  • taking the blood thinning drug warfarin

Stop use and ask a doctor if

  • pain gets worse or lasts more than 10 days in adults and children
  • pain gets worse or lasts more than 5 days in children under 12
  • 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 tablets every 4 to
6 hours while symptoms last

do not take more than 12
tablets in 24 hours

do not take for more than
10 days unless directed
by a doctor 
children
6-11
years
take 1 tablet every 4 to 6 hours
while symptoms last

do not take more than 5 tablets
in 24 hours

do not take for more than 5 days
unless directed by a doctor 
children
under
6 years
do not use this adult regular
strength product in children under
6 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 (50°-86°F)
  • see end flap for expiration date and lot number

Inactive ingredients

povidone, starch, stearic acid

Principal Display Panel

Pain Reliever/Fever Reducer Compare to the Active Ingredient in Regular Strength Tylenol®† Our Family® Quality Care Since 1904 PAIN RELIEVERACETAMINOPHEN REGULAR STRENGTH 100 TABLETS 325 mg EACH TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING †This product is not manufactured or distributed by McNeil Consumer Healthcare, owner of the registered trademark Regular Strength Tylenol®. 50844    ORG11210412 DISTRIBUTED BYNASH FINCH COMPANY ©2004, 1996NFC BRANDS7600 FRANCE AVE S, MLPS, MN 55435www.ourfamilyfoods.com     NF16427 
104-12

104-12

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ACETAMINOPHEN 
acetaminophen  tablet
Product Information
Product Type HUMAN OTC DRUG NDC Product Code (Source) 70253-104
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ACETAMINOPHEN (ACETAMINOPHEN) ACETAMINOPHEN 325 mg
Inactive Ingredients
Ingredient Name Strength
STEARIC ACID  
Product Characteristics
Color WHITE Score no score
Shape ROUND Size 11mm
Flavor Imprint Code 44;104
Contains     
Packaging
# NDC Package Description Multilevel Packaging
1 70253-104-12 1 BOTTLE In 1 CARTON contains a BOTTLE
1 100 TABLET In 1 BOTTLE This package is contained within the CARTON (70253-104-12)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part343 07/13/1990

Labeler - NASH-FINCH COMPANY (006962294)
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 038154464 PACK
Establishment
Name Address ID/FEI Operations
LNK International, Inc. 832867894 MANUFACTURE
Revised: 08/2012NASH-FINCH COMPANY