Drugplain

Robitussin Honey Cough DM Day Night Value Pack

dextromethorphan HBr, guaifenesin, doxylamine succinate · KIT · Haleon US Holdings LLC

No Recall History
Plain English

Robitussin Honey Cough DM Day Night Value Pack is an over-the-counter combination product that contains dextromethorphan (a cough suppressant), guaifenesin (an expectorant to help thin mucus), and doxylamine (a sleep aid) to help relieve cough and cold symptoms day and night. This kit is designed to provide cough relief during the day and additional symptom relief at night with the added sleep aid.

Key Facts

Brand Name
Robitussin Honey Cough DM Day Night Value Pack
Generic Name
dextromethorphan HBr, guaifenesin, doxylamine succinate
NDC Code (Product)
0031-2059
Manufacturer
Haleon US Holdings LLC
Dosage Form
KIT
Marketing Status
Application #
M012
Marketing Start
04/30/2019

Recall History

No Recall History

Side Effects Reported to FDA

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

pneumonia52 reports
dyspnoea44 reports
nausea37 reports
cough35 reports
pyrexia29 reports
vomiting29 reports
fatigue27 reports
dizziness26 reports
diarrhoea22 reports
hypotension22 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses – Robitussin Honey Maximum Strength Cough + Chest Congestion DM temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

Dosage & Administration

Directions – Robitussin Honey Maximum Strength Cough + Chest Congestion DM do not take more than 6 doses in any 24-hour period measure only with dosing cup provided keep dosing cup with product mL = milliliter this adult product is not intended for use in children under 12 years of age age dose adults and children 12 years and over 20 mL every 4 hours children under 12 years do not use

Warnings

Warnings – Robitussin Honey Maximum Strength Cough + Chest Congestion DM Click here to enter Warnings Do not use 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 MOAI 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 cough that occurs with too much phlegm (mucus) cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis, or emphysema Stop use and ask a doctor if cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Frequently Asked Questions

What is Robitussin Honey Cough DM Day Night Value Pack used for?

Robitussin Honey Cough DM Day Night Value Pack is an over-the-counter combination product that contains dextromethorphan (a cough suppressant), guaifenesin (an expectorant to help thin mucus), and doxylamine (a sleep aid) to help relieve cough and cold symptoms day and night. This kit is designed to provide cough relief during the day and additional symptom relief at night with the added sleep aid.

Is Robitussin Honey Cough DM Day Night Value Pack a controlled substance?

Robitussin Honey Cough DM Day Night Value Pack is not classified as a controlled substance by the DEA.

What is the generic name for Robitussin Honey Cough DM Day Night Value Pack?

The generic name for Robitussin Honey Cough DM Day Night Value Pack is dextromethorphan HBr, guaifenesin, doxylamine succinate. There are 1 other brand versions of dextromethorphan HBr, guaifenesin, doxylamine succinate.

What is the NDC code for Robitussin Honey Cough DM Day Night Value Pack ?

The NDC (National Drug Code) for Robitussin Honey Cough DM Day Night Value Pack is 0031-2059, listed by Haleon US Holdings LLC.

Product NDC

0031-2059

Package NDC

0031-2059-01

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

Data from openFDA · Public domain (CC0 1.0)