PURGENLABS ACETAMINOPHEN- actaminophen liquid 
Advanced Rx LLC

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Active Ingredient

in each 15 mL Tablespoonful

Acetaminophen 500 mg

Purpose

Pain Reliever/Fever Reducer

Uses

Warnings

Liver Warning:This product contains acetaminophen. The maximurr
daily dose of fhis product is 6 tablespoonfuls in 24 hours.
Severe liver damage may occur if you take
• more than 8 tablespoonfuls (4,000 mg of acetaminophen) in 24
hours • 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.

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

Ask a doctor before use ff rou have liver disease.
Ask a doctor before use ff you are taking the blood thinning
drug wartarin.
When using this product Do not exceed recommended dose.

Stop use and ask a doctor If • pain gets worse or lasts more than
10 days • fever gets worse or lasts more than 3 days • new
symptoms occur • redness or swelling is present.
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. 

 AgeDose 
 adults and children 12 years of age and olderTake 1 to 2 Tablespoonfuls every 4 to 6 hours as needed; not more than 6 tablespoonsfuls in 24 hours 
 children under 12 years Do not use 

Inactive ingredients: artificial and natural cherry flavor, citric acid, FD&C Red #40, methylparaben, polyethylene glycol, propylene glycol, propylparaben, purified water, sodium citrate, sucralose

Questions or comments? call toll free 1-800-630-8895

APAP

PURGENLABS ACETAMINOPHEN 
actaminophen liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80513-230
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN500 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
WATER (UNII: 059QF0KO0R)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:80513-230-081 in 1 CARTON06/01/2024
1237 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01206/01/2024
Labeler - Advanced Rx LLC (042795108)

Revised: 6/2024
Document Id: a8ae2ac6-f3b4-458b-acbb-fa4ff186503c
Set id: 915c4608-af1b-4119-8291-4ce9fd701d76
Version: 1
Effective Time: 20240628
 
Advanced Rx LLC