EXTRA STRENGTH MAPAP- acetaminophen tablet 
Preferred Pharmaceuticals, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Mapap (Acetaminophen) Extra Strength Tablets

Drug Facts

Active ingredient (in each tablet)

Acetaminophen 500 mg

Purposes

Pain Reliever/Fever Reducer

Uses

for the temporary relief of 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

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

more than 4,000 mg of acetaminophen in 24 hours
with other drugs containing acetaminophen
3 or more alcoholic drinks every day while using this product

Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include:

skin reddening
blisters
rash

If a skin reaction occurs, stop use and seek medical help right away.

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.
if you are allergic to acetaminophen or any of the inactive ingredients in this product

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: In the 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 the directed (see overdose warning)
adults and children 12 years and over:
take 2 tablets every 6 hours while symptoms last.
do not take more than 6 tablets in 24 hours unless directed by a doctor
do not take for more than 10 days unless directed by a doctor

children under 12 years: ask a doctor

Other information

Store at room temperature

Inactive ingredients Povidone, pregelatinized starch, sodium starch glycolate, stearic acid.

Questions or comments? Call (800) 616-2471

Distributed By: MAJOR® PHARMACEUTICALS

17177 N. Laurel Park Drive, Suite 233, Livonia, MI 48152 USA

Do not use if carton is open, or if imprinted safety seal under cap is broken or missing

Repackaged By: Preferred Pharmaceuticals Inc.

MAJOR®

NDC 68788-9394

See New Warnings Information and Directions

EXTRA STRENGTH

Mapap TABLETS

ASPIRIN FREE

STRONG PAIN AND FEVER RELIEF

500 MG EACH

Repackaged By: Preferred Pharmaceuticals Inc.

Extra Strenght Acetaminophen 500mg
EXTRA STRENGTH MAPAP 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68788-9394(NDC:0904-1988)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg
Inactive Ingredients
Ingredient NameStrength
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
Product Characteristics
ColorWHITEScore2 pieces
ShapeROUND (round flat faced beveled edge) Size12mm
FlavorImprint Code GPI;A5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68788-9394-220 in 1 BOTTLE; Type 0: Not a Combination Product06/24/201405/03/2021
2NDC:68788-9394-330 in 1 BOTTLE; Type 0: Not a Combination Product06/24/201405/03/2021
3NDC:68788-9394-445 in 1 BOTTLE; Type 0: Not a Combination Product06/24/201405/03/2021
4NDC:68788-9394-550 in 1 BOTTLE; Type 0: Not a Combination Product06/24/201405/03/2021
5NDC:68788-9394-1100 in 1 BOTTLE; Type 0: Not a Combination Product06/24/201405/03/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34306/24/201405/03/2021
Labeler - Preferred Pharmaceuticals, Inc. (791119022)
Registrant - Preferred Pharmaceuticals, Inc. (791119022)
Establishment
NameAddressID/FEIBusiness Operations
Preferred Pharmaceuticals, Inc.791119022REPACK(68788-9394)

Revised: 5/2021
 
Preferred Pharmaceuticals, Inc.