Drugplain

VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU

Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate · KIT · The Procter & Gamble Manufacturing Company

No Recall HistoryCurrently in Shortage
Plain English

VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU is a kit containing acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and doxylamine succinate, taken oral. Manufactured by The Procter & Gamble Manufacturing Company.

Key Facts

Brand Name
VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU
Generic Name
Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate
NDC Code (Product)
69423-808
Manufacturer
The Procter & Gamble Manufacturing Company
Dosage Form
KIT
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
04/28/2020

Recall History

No Recall History

Frequently Asked Questions

What is VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU used for?

VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU contains Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate. It is a kit taken oral. Consult your doctor for specific uses.

Is VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU a controlled substance?

VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU is not classified as a controlled substance by the DEA.

What is the generic name for VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU?

The generic name for VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU is Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate. There are 1 other brand versions of Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl and Doxylamine succinate.

What is the NDC code for VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU ?

The NDC (National Drug Code) for VICKS DayQuil SEVERE NyQuil SEVERE HONEY FLAVOR COLD and FLU is 69423-808, listed by The Procter & Gamble Manufacturing Company.

Product NDC

69423-808

Package NDC

69423-808-24

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

Data from openFDA · Public domain (CC0 1.0)