Childrens MAPAP Acetaminophen

Manufacturer
Atlantic Biologicals Corps
Effective date
2019-10-18
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:01:00

Label at a glance#

ProductChildrens MAPAP Acetaminophen
Active ingredientAcetaminophen
Label structure9 sections

Indications and uses

Temporarily relieves minor aches and pains due to: the common cold flu headache sore throat toothache Temporarily reduces fever

Dosage and administration

this product does not contain directions or complete warnings for adult use find right dose on chart if possible, use weight to dose; otherwise, use age if needed, repeat dose every 4 hours do not use more than 5 doses in 24 hours Weight Age Dose under 24 lbs Under 2 years ask a doctor 24 to 35 lbs 2 to 3 years 1 TSP (5 mL) 36 to 47 lbs 4 to 5 years 1 1/2 TSP (7.5 mL) 48 to 59 lbs 6 to 8 years 2 TSP (10 mL) 60 to ...

Storage and handling

sodium 1mg Each TSP(5 mL) contains: TAMPER-EVIDENT: Do not use this product if inner foil seal over mouth of the bottle is cut, torn, broken, or missing. store at 20° - 25°C (68° – 77°F) this product is not the same concentration as Infants' Drops. For accurate dosing, follow the dosing instructions on this label.

Label contents#

Full prescribing information#

Active ingredient (in each TSP (5 mL))

OTC - ACTIVE INGREDIENT SECTION

Acetaminophen 160 mg

Purpose

OTC - PURPOSE SECTION

Fever reducer-Pain reliever

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains due to:

  • the common cold
  • flu
  • headache
  • sore throat
  • toothache

Temporarily reduces fever

Warnings

WARNINGS SECTION

Liver warning

SPL UNCLASSIFIED SECTION

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

Sore throat warning

SPL UNCLASSIFIED SECTION

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

OTC - DO NOT USE SECTION

  • with any other product containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist

OTC - ASK DOCTOR SECTION

liver disease Ask a doctor before use if your child has

OTC - ASK DOCTOR/PHARMACIST SECTION

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

OTC - STOP USE SECTION

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.

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use If pregnant or breast-feeding,

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

Overdose warning

SPL UNCLASSIFIED SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • this product does not contain directions or complete warnings for adult use
  • find right dose on chart
  • if possible, use weight to dose; otherwise, use age
  • if needed, repeat dose every 4 hours
  • do not use more than 5 doses in 24 hours
WeightAgeDose
under 24 lbsUnder 2 yearsask a doctor
24 to 35 lbs2 to 3 years1 TSP (5 mL)
36 to 47 lbs4 to 5 years1 1/2 TSP (7.5 mL)
48 to 59 lbs6 to 8 years2 TSP (10 mL)
60 to 71 lbs9 to 10 years2 1/2 TSP (12.5 mL)
72 to 95 lbs11 years3 TSP (15 mL)

Other information

STORAGE AND HANDLING SECTION

  • sodium 1mg Each TSP(5 mL) contains:
  • TAMPER-EVIDENT: Do not use this product if inner foil seal over mouth of the bottle is cut, torn, broken, or missing.
  • store at 20° - 25°C (68° – 77°F)
  • this product is not the same concentration as Infants' Drops. For accurate dosing, follow the dosing instructions on this label.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

Questions?

OTC - QUESTIONS SECTION

To Report Adverse Drug Event call 1-800-616-2471 Weekdays, 9AM - 5PM Eastern Time

CHILDRENS MAPAP ACETAMINOPHEN (ACETAMINOPHEN) LIQUID

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
307675acetaminophen 160 MG in 5 mL Oral SolutionPSN3
209397Mapap Childrens 160 MG in 5 mL Oral SolutionPSN3
209397acetaminophen 32 MG/ML Oral Solution [Mapap]SBD3
307675acetaminophen 32 MG/ML Oral SolutionSCD3
307675acetaminophen 160 MG per 5 ML Oral SolutionSY3
307675acetaminophen 325 MG per 10.15 ML Oral SolutionSY3
307675acetaminophen 650 MG per 20.3 ML Oral SolutionSY3
307675acetaminophen 80 MG per 2.5 ML Oral SolutionSY3
307675APAP 32 MG/ML Oral SolutionSY3
209397APAP 32 MG/ML Oral Solution [Mapap]SY3
209397Mapap 160 mg per 5 mL Oral SolutionSY3
209397Mapap 32 MG/ML Oral SolutionSY3

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17856-1985-1Childrens MAPAP Acetaminophen5 mL in 1 CUPLIQUID53
17856-1985-5Childrens MAPAP Acetaminophen5 mL in 1 CUPLIQUID53
17856-1985-9Childrens MAPAP Acetaminophen1 mL in 1 SYRINGELIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17856-1985CHILDRENS MAPAP ACETAMINOPHEN (ACETAMINOPHEN) LIQUID [ATLANTIC BIOLOGICALS CORPS]3Legacy NDC, 3 package rows20191019_5fb6ac05-fd0f-400f-9563-e0273c6b7ce5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
17856-1985-9ML - Milliliter17856-19858a479d35-1b82-45a3-a05c-bcaf559c9ec312016-09-02
0904-1985-00ML - Milliliter0904-19853a7ef64c-8df0-4322-a91f-f54e0f3c9d3612013-02-13
0904-1985-16ML - Milliliter0904-19852906032b-7c3a-4872-b7e9-695aa95d6c1b12013-02-13
0904-1985-20ML - Milliliter0904-19853cbd29ae-733e-42cf-92cb-f21c9b56f98012013-02-13

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
17856-198517856-1985-1, 17856-1985-5, 17856-1985-9
0904-1985

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f9b43095-0ce7-4f9c-ab83-06bd5989263b5fb6ac05-fd0f-400f-9563-e0273c6b7ce52019-10-18WarningsExact identifier
spl id: f9b43095-0ce7-4f9c-ab83-06bd5989263b
spl set id: 5fb6ac05-fd0f-400f-9563-e0273c6b7ce5

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.