EXTRA STRENGTH MAPAP- acetaminophen tablet 
Aidarex Pharmaceuticals LLC

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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Drug Facts

Active ingredient (in each tablet)

Acetaminophen 500 mg

Purposes

Pain Reliever/Fever Reducer

Aspirin Free Extra Strength Pain Reliever

Uses

for the temporary relief of minor aches and pains due to:

Warnings

Liver warning: This product contains acetaminophen.

The maximum daily dose of this product is 6 tablets (3,000mg) in 24 hours.  Severe liver damage may occur if you take

Do not use

  • •with any other drug containing acetaminophen (prescription or non prescription). 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

This Unit Dose package is not child resistant and is Intended for Institutional Use Only.

Overdose warning: Taking more than the recommended dose (overdose) may cause liver damage. 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:

Children under 12 years: Do not use adult Extra Strength product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage.

Other information

Inactive ingredients

Povidone, Pregelatinized Starch, Sodium Starch Glycolate, Stearic Acid

Questions or comments?

To report Adverse Drug Event call (800) 616-2471

Tamper Evident:

 Do not use if sealed blister units are broken or damaged.

Repackaged By:

Aidarex Pharmaceuticals, LLC

Corona, CA 92880

Principal Display Panel

NDC 0904-1988-59

See New Warnings Information and Directions

EXTRA STRENGTH

Mapap TABLETS

ASPIRIN FREE

STRONG PAIN AND FEVER RELIEF

Mapap ES 500mg tablet

Mapap ES 500mg tablet

EXTRA STRENGTH MAPAP 
acetaminophen tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:33261-003(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 CORN (UNII: AG9B65PV6B)  
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:33261-003-00100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
2NDC:33261-003-2020 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
3NDC:33261-003-3030 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
4NDC:33261-003-4040 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
5NDC:33261-003-4545 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
6NDC:33261-003-5050 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
7NDC:33261-003-6060 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/04/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34305/04/2011
Labeler - Aidarex Pharmaceuticals LLC (801503249)

Revised: 8/2017
Document Id: feac2096-3a09-478f-9c0d-349eb3707e57
Set id: c952efb5-2bac-4304-a422-a60c36bba496
Version: 1
Effective Time: 20170818
 
Aidarex Pharmaceuticals LLC