FDA.reportPublic FDA data

M-PAP

Manufacturer
Bryant Ranch Prepack
Effective date
2026-03-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:50:36

Label at a glance#

ProductM-PAP
Active ingredientACETAMINOPHEN
Label structure11 sections

Indications and uses

reduces fever temporarily relieves minor aches and pains due to: Headache muscular aches backache arthritis the common cold toothache menstrual cramps reduces fever

Dosage and administration

Do not exceed recommended dosage. adults and children 12 years of age and older: Take 3 teaspoonfuls (15 mL) every 5 hours; do not exceed 15 teaspoonfuls (75 mL) in 24 hours children under 12 years of age: Under the direct guidance of a licensed professional, doctor, or pharmacist.

Storage and handling

each 5 mL contains: Sodium 3 mL If dispensed, dispense in a tight, light resistant cotainer with a child-resistant cap. Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

M-PAP

Acetaminophen Liquid

160 mg/5 mL

Pain Reliever / Fever Reducer

Sugar Free / Alcohol Free

Aspirin Free

CHERRY FLAVOR

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

(in each 5 mL teaspoonful)

Acetaminophen, USP 160 mg ....................

Purpose

OTC - PURPOSE SECTION

Pain reliever/fever reducer

Uses

INDICATIONS & USAGE SECTION

  • reduces fever
  • temporarily relieves minor aches and pains due to:
    • Headache
    • muscular aches
    • backache
    • arthritis
    • the common cold
    • toothache
    • menstrual cramps
    • reduces fever

Warnings

WARNINGS SECTION

Liver Warning: This product contains acetaminophen.

Severe liver damage may occur if you take:

  • more than 8 teaspoonfuls (40 mL) in 24 hours, which is the maximum daily amount
  • 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.

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

OTC - DO NOT USE SECTION

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

  • for more than 10 days for pain unless directed by a doctor
  • for more than 3 days for fever unless directed by a doctor
  • if you are allergic to acetaminophen or any of the inactive ingredients in this product.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have health issues especially liver disease.

Ask a doctor or pharmacist before use

OTC - ASK DOCTOR/PHARMACIST SECTION

if you are taking other drugs, including the blood thinner warfarin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • new symptoms occur such as rash, hives, itching or hoarseness
  • redness or swelling is present
  • pain gets worse or lasts for more than 10 days
  • fever gets worse or lasts for more than 3 days
  • symptoms do not improve

These could be signs of a serious condition.

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children. Overdose warning

OTC - KEEP OUT OF REACH OF CHILDREN 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 right away. Prompt medical attention is critical even if you do not notice any signs or symptoms.

Directions

DOSAGE & ADMINISTRATION SECTION

Do not exceed recommended dosage.

  • adults and children 12 years of age and older: Take 3 teaspoonfuls (15 mL) every 5 hours; do not exceed 15 teaspoonfuls (75 mL) in 24 hours
  • children under 12 years of age: Under the direct guidance of a licensed professional, doctor, or pharmacist.

Other Information

STORAGE AND HANDLING SECTION

  • each 5 mL contains: Sodium 3 mL

If dispensed, dispense in a tight, light resistant cotainer with a child-resistant cap. Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Anhydrous citric acid, FD&C Blue #1, FD&C Red #40, flavor, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, saccharin sodium, sodium benzoate, sorbitol solution.

Questions?

OTC - QUESTIONS SECTION

1-877-250-3427 M-F (8 a.m. to 5 p.m. CST), or directly to Medwatch at 1-800-332-1088.

Serious side effects associated with use of this product may be reported to this number.

Distributed by:

Method Pharmaceuticals

Southlake, TX 76092

Rev. 02/2024

HOW SUPPLIED

How Supplied Section

M-PAP Acetaminophen Liquid 160 mg/5 ml

NDC: 72162-2404-2: 473 mL in a BOTTLE
NDC: 72162-2404-4: 118 mL in a BOTTLE

If dispensed, dispense in a tight, light resistant cotainer with a child-resistant cap. Store at 20°C to 25°C (68°F to 77°F), excursions permitted between 15°C and 30°C (between 59°F and 86°F).

Repackaged/Relabeled by:

Bryant Ranch Prepack
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

M-PAP Oral Liquid 160mg/5ml #473

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
307675acetaminophen 160 MG in 5 mL Oral SolutionPSN3
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

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedailymed.nlm.nih.gov/dailymed/search.cfm?query=72162-2404-4lbl721622404.jpg
Data codeCode 1287216224044lbl721622404.jpg
Data codeData Matrix lbl721622404.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-2404-2M-PAP473 mL in 1 BOTTLELIQUID4733
72162-2404-4M-PAP118 mL in 1 BOTTLELIQUID1183

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-2404-2ML - Milliliter72162-24049dc22ea3-92b3-4b03-8f7d-c1979501e84a12024-12-10
72162-2404-4ML - Milliliter72162-24042895709e-da44-4546-8332-f743ba492d2f12025-05-14
58657-524-04ML - Milliliter58657-52461cca8ca-d3d3-4387-a446-52a2492aa7bf12024-05-16
58657-524-16ML - Milliliter58657-52447a56d48-9746-42a0-82be-38c8e9a6382d12024-05-16

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72162-240472162-2404-2, 72162-2404-4
58657-524

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
WATER059QF0KO0RIACT
SODIUM BENZOATEOJ245FE5EUIACT
SACCHARIN SODIUMSB8ZUX40TYIACT
SORBITOL506T60A25RIACT
ACETAMINOPHEN362O9ITL9DACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
FD&C RED NO. 40WZB9127XOAIACT
HIGH FRUCTOSE CORN SYRUPXY6UN3QB6SIACT

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
M-PAPACETAMINOPHENBryant Ranch Prepackc6cec390-004e-45f6-9388-c662a979f37d2026-03-17WarningsExact identifier
ndc (package): 72162-2404-4
ndc (package): 72162-2404-2
ndc (product): 72162-2404
ndc11 (package): 72162240404
ndc11 (package): 72162240402
spl id: b7edfaf9-8bf5-4caa-aa48-f3ca3cc06eb7
spl set id: c6cec390-004e-45f6-9388-c662a979f37d
M-PAPACETAMINOPHENMethod Pharmaceuticals, LLC1539dc44-15a0-153b-e063-6294a90a9d452025-10-21WarningsExact identifier
ndc (product): 58657-524

Reported adverse events (FAERS/openFDA)#

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