CHILDRENS MAPAP- acetaminophen liquid 
Central Texas Community Health Centers

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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Children's Māpap® ACETAMINOPHEN LIQUID

Drug Facts

Active ingredient (in each 5mL)

Acetaminophen 160 mg

Purpose

Pain reliever - Fever reducer

Uses

Temporarily relieves minor aches and pains due to:

Temporarily reduces fever

Warnings

Liver warning

This product contains acetaminophen. Severe liver damage may occur if your child takes:

  • more than 5 doses in 24 hours, which is the maximum daily amount
  • with other drugs containing acetaminophen

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.

Sore throat warning

If sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly.

Do not use

  • with any other product containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist
  • if your child is allergic to acetaminophen or any of the inactive ingredients in this product

Ask a doctor before use if your child has liver disease

Ask a doctor or pharmacist before use if your child is taking the blood thinning drug warfarin.

When using this product, do not exceed recommended dose (see overdose warning)

Stop use and ask a doctor if

  • pain gets worse or last for more than 5 days
  • fever gets worse or last for more than 3 days
  • new symptoms occur
  • redness or swelling is present

These could be signs of a serious condition.

Keep out of the 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 (1-800-222-1222) right away. Quick medical attention is critical for adults as well as children even if you do not notice any signs or symptoms.

Directions

WeightAgeDose
under 24 lbsUnder 2 yearsask a doctor
24 to 35 lbs2 to 3 years5mL
36 to 47 lbs4 to 5 years7.5mL
48 to 59 lbs6 to 8 years10mL
60 to 71 lbs9 to 10 years12.5mL
72 to 95 lbs11 years15mL

Other information

Inactive ingredients

artificial flavor, citric acid anhydrous, D&C Red #33, FD&C Red #40, glycerin, polyethylene glycol 1450, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol

Questions or Comments?

Call 1-800-616-2471

PRINCIPAL DISPLAY PANEL - 118 ML Bottle Label

Austin/Travis Co. Health & Human Services Dept.
1000 Toyath St Austin, TX 78702 512-972-6206

MAPAP
160 mg/5
ML
#118ML

Date:

Name:
Dr.

TAKE ___ ML BY MOUTH ___ TIMES A DAY.

12/2018

16M021

MAPAP 160 mg/5 ML #118ML NDC 76413-343-01

Batch: 08301709
Lot: 16M021
Exp: 12/2018
MAJOR

Federal law prohibits the transfer of this drug to any other person than the patient for whom prescribed.

PRINCIPAL DISPLAY PANEL - 118 ML Bottle Label
CHILDRENS MAPAP 
acetaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76413-343(NDC:0904-1985)
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen160 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
Glycerin (UNII: PDC6A3C0OX)  
Sorbitol (UNII: 506T60A25R)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Anhydrous citric acid (UNII: XF417D3PSL)  
FD&C Red no. 40 (UNII: WZB9127XOA)  
Water (UNII: 059QF0KO0R)  
saccharin sodium (UNII: SB8ZUX40TY)  
Propylene glycol (UNII: 6DC9Q167V3)  
PRUNUS SEROTINA BARK (UNII: 5D48E975HA)  
POLYETHYLENE GLYCOL 1450 (UNII: OJ4Z5Z32L4)  
D&C RED NO. 33 (UNII: 9DBA0SBB0L)  
Product Characteristics
ColorREDScore    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:76413-343-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product03/01/2015
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34303/01/2015
Labeler - Central Texas Community Health Centers (079674019)
Establishment
NameAddressID/FEIBusiness Operations
Central Texas Community Health Centers079674019REPACK(76413-343) , RELABEL(76413-343)

Revised: 9/2017
Document Id: 6dc153b5-8e73-4c2b-b760-302f6954e701
Set id: 8259aefb-88bf-4adb-8ada-8a33e1ffa26d
Version: 1
Effective Time: 20170908
 
Central Texas Community Health Centers