Drugplain

Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 325 mg/1

Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride · CAPSULE, LIQUID FILLED · SOFTGEL HEALTHCARE PRIVATE LIMITED

No Recall HistoryCurrently in Shortage
Plain English

Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride is a capsule, liquid filled containing acetaminophen, dextromethorphan hydrobromide and phenylephrine hydrochloride at 325 mg/1, taken oral. Manufactured by SOFTGEL HEALTHCARE PRIVATE LIMITED.

Key Facts

Brand Name
Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride
Generic Name
Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride
NDC Code (Product)
35916-0917
Manufacturer
SOFTGEL HEALTHCARE PRIVATE LIMITED
Strength
325 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
06/19/2025

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

aspartate aminotransferase increased1 reports
jaundice1 reports
myocardial infarction1 reports
potentiating drug interaction1 reports
transaminases increased1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses Temporarily relieves common cold/flu symptoms: nasal congestion cough due to minor throat & bronchial irritation sore throat headache minor aches & pains fever

Dosage & Administration

Directions take only as directed do not exceed 8 Softgels per 24 hrs adults & children 12 years & over 2 Softgels with water every 4 hours children 4 to under 12 years ask a doctor children under 4 years do not use

Warnings

Warnings Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 8 Softgels in 24 hrs, which is the maximum daily amount for this product 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. 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.

Frequently Asked Questions

What is Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride used for?

Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride contains Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride a controlled substance?

Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride is not classified as a controlled substance by the DEA.

What is the generic name for Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride?

The generic name for Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride is Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride. There are no other listed brand versions of Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride.

What is the NDC code for Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 325 mg/1?

The NDC (National Drug Code) for Acetaminophen, Dextromethorphan Hydrobromide and Phenylephrine Hydrochloride 325 mg/1 is 35916-0917, listed by SOFTGEL HEALTHCARE PRIVATE LIMITED.

Product NDC

35916-0917

Package NDC

35916-0917-1

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)