M-PAP - Bryant Ranch Prepack

Manufacturer
Bryant Ranch Prepack
Effective date
2026-03-25
Label type
HUMAN OTC DRUG LABEL
Version
101
Source
full-release
Hydrated at
2026-06-01 01:51:44

Label at a glance#

ProductM-PAP
Active ingredientACETAMINOPHEN
Label structure11 sections

Indications and uses

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. Overdose Warnings: Taking more than the recommended dose (overdose) can cause serious health problems, including liver damage.  adults and children 12 years of age and older: take 2 teaspoonfuls (10 mL) every 6 hours; do not exceed 8 teaspoonfuls (40 mL) in 24 hours  children under 12 years of age: Under the direct guidance of a licensed professional, doctor, or pharmacist.

Storage and handling

If dispensed, dispense in a tight, light resistant container 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

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.

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.

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.

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

Overdose Warnings: Taking more than the recommended dose (overdose) can cause serious health problems, including liver damage. 

  • adults and children 12 years of age and older: take 2 teaspoonfuls (10 mL) every 6 hours; do not exceed

8 teaspoonfuls (40 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

If dispensed, dispense in a tight, light resistant container 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

Bitter Mask, Cherry Flavor, Citric Acid, FD&C Red No. 40, Glycerin, Polyethylene Glycol, Purified Water, Sodium Benzoate, Sodium Citrate Dihydrate, Sodium Saccharin, Sorbitol.

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.

See New Warnings Information

Tamper evident by foil seal under cap.

Do not use if foil seal is broken or missing.

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.

Distributed by:

Method Pharmaceuticals

Fort Worth, Texas 76118

Rev. 06/19

HOW SUPPLIED

How Supplied Section

M-PAP

Acetaminophen Liquid

160 mg/5 mL

NDC: 72162-1673-2: 120 mL in a BOTTLE

NDC: 72162-1673-4: 473 mL in a BOTTLE

Repackaged/Relabeled by:
Bryant Ranch Prepack
Burbank, CA 91504

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

M-PAP Oral Liquid 160 MG/5ML #120

Label
Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
307675acetaminophen 160 MG in 5 mL Oral SolutionPSN101
307675acetaminophen 32 MG/ML Oral SolutionSCD101
307675acetaminophen 160 MG per 5 ML Oral SolutionSY101
307675acetaminophen 325 MG per 10.15 ML Oral SolutionSY101
307675acetaminophen 650 MG per 20.3 ML Oral SolutionSY101
307675acetaminophen 80 MG per 2.5 ML Oral SolutionSY101
307675APAP 32 MG/ML Oral SolutionSY101

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedailymed.nlm.nih.gov/dailymed/search.cfm?adv=1&query=NDC:72162-1673-2lbl721621673.jpg
Data codeCode 1287216216732lbl721621673.jpg
Data codeData Matrix lbl721621673.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1673-2M-PAP120 mL in 1 BOTTLELIQUID120101
72162-1673-4M-PAP473 mL in 1 BOTTLELIQUID473101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1673-2ML - Milliliter72162-16738056e9ec-7c77-42b2-b081-8f8819c8d73012024-09-09
72162-1673-4ML - Milliliter72162-1673e679dbb5-6be5-44dd-8720-39ee2beed10512024-09-09
58657-525-04ML - Milliliter58657-52564573b7b-b406-4e75-a90e-4f58d9aa56d412019-09-05
58657-525-16ML - Milliliter58657-5256b398395-119f-4ccf-9f37-9fffa24d434112019-09-05

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72162-167372162-1673-2, 72162-1673-4
58657-525

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
M-PAPACETAMINOPHENBryant Ranch Prepackad01aea6-4af3-469b-b99d-e1e66aa40e8d2026-03-25WarningsExact identifier
ndc (package): 72162-1673-4
ndc (package): 72162-1673-2
ndc (product): 72162-1673
ndc11 (package): 72162167304
ndc11 (package): 72162167302
spl id: 29268c14-1ad1-4793-b892-582d39122284
spl set id: ad01aea6-4af3-469b-b99d-e1e66aa40e8d
M-PAPACETAMINOPHENMethod Pharmaceuticals, LLC3d1bb61c-15db-4eba-aba9-cfbcbc7b30e02025-10-21WarningsExact identifier
ndc (product): 58657-525

Reported adverse events (FAERS/openFDA)#

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