Sudafed PE Sinus Pressure Plus Pain 325 mg/1
Acetaminophen and Phenylephrine hydrochloride · TABLET, FILM COATED · Kenvue Brands LLC
Sudafed PE Sinus Pressure Plus Pain is a tablet, film coated containing acetaminophen and phenylephrine hydrochloride at 325 mg/1, taken oral. Manufactured by Kenvue Brands LLC.
Key Facts
- Brand Name
- Sudafed PE Sinus Pressure Plus Pain
- Generic Name
- Acetaminophen and Phenylephrine hydrochloride
- NDC Code (Product)
50580-435- Manufacturer
- Kenvue Brands LLC
- Strength
- 325 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- M012
- Marketing Start
- 06/17/2019
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
Uses temporarily relieves these symptoms associated with hay fever or other respiratory allergies, and the common cold: sinus congestion and pressure headache minor aches and pains nasal congestion promotes sinus drainage temporarily reduces fever
Dosage & Administration
Directions do not use more than directed (see overdose warning ) adults and children 12 years and over take 2 tablets every 4 hours do not take more than 10 tablets in 24 hours children under 12 years ask a doctor
Warnings
Warnings Liver warning This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg acetaminophen) in 24 hours. Severe liver damage may occur if you take more than 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 doctor or pharmacist. if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson's disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. if you have ever had an allergic reaction to this product or any of its ingredients Ask a doctor before use if you have liver disease heart disease high blood pressur…
Frequently Asked Questions
What is Sudafed PE Sinus Pressure Plus Pain used for?
Sudafed PE Sinus Pressure Plus Pain contains Acetaminophen and Phenylephrine hydrochloride. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Sudafed PE Sinus Pressure Plus Pain a controlled substance?
Sudafed PE Sinus Pressure Plus Pain is not classified as a controlled substance by the DEA.
What is the generic name for Sudafed PE Sinus Pressure Plus Pain?
The generic name for Sudafed PE Sinus Pressure Plus Pain is Acetaminophen and Phenylephrine hydrochloride. There are 10 other brand versions of Acetaminophen and Phenylephrine hydrochloride.
What is the NDC code for Sudafed PE Sinus Pressure Plus Pain 325 mg/1?
The NDC (National Drug Code) for Sudafed PE Sinus Pressure Plus Pain 325 mg/1 is 50580-435, listed by Kenvue Brands LLC.
Other Sudafed PE Sinus Pressure Plus Pain Dosages
Other Acetaminophen Brands
See all →- SUDAFED PE Pressure Plus Pain325 mg/150580-547
- Sinus Pressure plus Pain PE325 mg/163941-220
- Sinus Pressure plus Pain PE325 mg/168998-220
- sinus pressure and pain pe325 mg/150804-220
- Sinus plus Headache325 mg/168998-323
- Sinus Pressure plus Pain PE325 mg/172036-320
- Sinus plus Headache325 mg/172036-323
- SINUS AND HEADACHE325 mg/172476-123
- Sinus Pressure and Pain PE325 mg/142507-320
- Sinus and Headache325 mg/157344-923
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)