Drugplain

Sanaflu Xtra 250 mg/1

ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE · CAPSULE, GELATIN COATED · GRANDALL DISTRIBUTING, LLC

No Recall HistoryCurrently in Shortage
Plain English

Sanaflu Xtra is a capsule, gelatin coated containing acetaminophen, chlorpheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride at 250 mg/1, taken oral. Manufactured by GRANDALL DISTRIBUTING, LLC.

Key Facts

Brand Name
Sanaflu Xtra
Generic Name
ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE
NDC Code (Product)
48201-001
Manufacturer
GRANDALL DISTRIBUTING, LLC
Strength
250 mg/1
Dosage Form
CAPSULE, GELATIN COATED
Route
ORAL
Marketing Status
Application #
M013
Marketing Start
04/30/2015

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relives minor aches and pains headache runny nose sneezing nasal congestion itchy, watery eyes due to hay fever or other upper respiratory allergies itching of the nose or throat cough due to minor throat and bronchial irritation as may occur with the common cold ro inhaled irritants Temperarily reduces fever

Dosage & Administration

Directions Adults and children 12 years of age and older: Take 2 capsules every 4 hours; not more than 12 capsules in 24 hours. Children under 12 years of age: Consult a doctor.

Warnings

Warnings Liver warning This product contains acetaminophen. 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. 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 monamine 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. Ask a doctor before use if you have liver disease a breathing problem such as emphysema or chronic bronchitis glaucoma heart disease high blood pressure difficulty in urination due to enlargement of the prostate gland persistant or chrnoic cough such as occurs with smoking, asthma, or emphysema cough accompanied by excessive phlegm thyroid disease diabetes Ask a doctor or pharmacist before use if you are taking the blood thinning drug

Frequently Asked Questions

What is Sanaflu Xtra used for?

Sanaflu Xtra contains ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE. It is a capsule, gelatin coated taken oral. Consult your doctor for specific uses.

Is Sanaflu Xtra a controlled substance?

Sanaflu Xtra is not classified as a controlled substance by the DEA.

What is the generic name for Sanaflu Xtra?

The generic name for Sanaflu Xtra is ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE. There are 8 other brand versions of ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE.

What is the NDC code for Sanaflu Xtra 250 mg/1?

The NDC (National Drug Code) for Sanaflu Xtra 250 mg/1 is 48201-001, listed by GRANDALL DISTRIBUTING, LLC.