Drugplain

DayTime Sinus Relief 325 mg/1

acetaminophen, phenylephrine hydrochloride · CAPSULE, LIQUID FILLED · Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.

No Recall HistoryCurrently in Shortage
Plain English

DayTime Sinus Relief is a capsule, liquid filled containing acetaminophen, phenylephrine hydrochloride at 325 mg/1, taken oral. Manufactured by Humanwell PuraCap Pharmaceutical (Wuhan), Ltd..

Key Facts

Brand Name
DayTime Sinus Relief
Generic Name
acetaminophen, phenylephrine hydrochloride
NDC Code (Product)
53345-012
Manufacturer
Humanwell PuraCap Pharmaceutical (Wuhan), Ltd.
Strength
325 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
06/15/2013

Recall History

No Recall History

Frequently Asked Questions

What is DayTime Sinus Relief used for?

DayTime Sinus Relief contains acetaminophen, phenylephrine hydrochloride. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is DayTime Sinus Relief a controlled substance?

DayTime Sinus Relief is not classified as a controlled substance by the DEA.

What is the generic name for DayTime Sinus Relief?

The generic name for DayTime Sinus Relief is acetaminophen, phenylephrine hydrochloride. There are 11 other brand versions of acetaminophen, phenylephrine hydrochloride.

What is the NDC code for DayTime Sinus Relief 325 mg/1?

The NDC (National Drug Code) for DayTime Sinus Relief 325 mg/1 is 53345-012, listed by Humanwell PuraCap Pharmaceutical (Wuhan), Ltd..