M-PAP- acetaminophen liquid 
Method Pharmaceuticals, LLC

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M-PAP

M-PAP

Acetaminophen Liquid

160 mg/5 mL

Pain Reliever / Fever Reducer

Sugar Free / Alcohol Free

Aspirin Free

CHERRY FLAVOR

Drug Facts

Active ingredient

(in each 5 mL teaspoonful)

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

Purpose

Pain reliever/fever reducer

Uses

Warnings

Liver Warning: This product contains acetaminophen.

Severe liver damage may occur if you take:

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

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 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

if you have health issues especially liver disease.

Ask a doctor or pharmacist before use

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

When using this product do no exceed recommended dose (see Overdose warning)

Stop use and ask a doctor if

  • 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,

ask a health professional before use.

Keep out of 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 right away. Prompt medical attention is critical even if you do not notice any signs or symptoms.

Directions

Do not exceed recommended dosage.

Other Information

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

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?

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

PRINCIPAL DISPLAY PANEL

NDC 58657-524-04

M-PAP

Acetaminophen Liquid

160 mg/5 mL

Cherry Flavor

4 fl. oz. (118mL)

label2

PRINCIPAL DISPLAY PANEL

NDC 58657-524-16

M-PAP

Acetaminophen Liquid

160 mg/5 mL

Cherry Flavor

16 fl. oz. (473 mL)

label1

M-PAP 
acetaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58657-524
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
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
WATER (UNII: 059QF0KO0R)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SORBITOL (UNII: 506T60A25R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
Product Characteristics
Color    Score    
ShapeSize
FlavorCHERRYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58657-524-04120 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2024
2NDC:58657-524-16473 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01304/01/2024
Labeler - Method Pharmaceuticals, LLC (060216698)

Revised: 4/2024
Document Id: 17e52c9c-c144-002d-e063-6294a90afeaa
Set id: 1539dc44-15a0-153b-e063-6294a90a9d45
Version: 2
Effective Time: 20240401
 
Method Pharmaceuticals, LLC