Drugplain

Rynex DM 1 mg/5mL

Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride · LIQUID · Edwards Pharmaceuticals, Inc

No Recall History
Plain English

Rynex DM is a liquid containing brompheniramine maleate, dextromethorphan hydrobromide, phenylephrine hydrochloride at 1 mg/5mL, taken oral. Manufactured by Edwards Pharmaceuticals, Inc.

Key Facts

Brand Name
Rynex DM
Generic Name
Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride
NDC Code (Product)
0485-0204
Manufacturer
Edwards Pharmaceuticals, Inc
Strength
1 mg/5mL
Dosage Form
LIQUID
Route
ORAL
Marketing Status
Application #
M012
Marketing Start
03/14/2011

Recall History

No Recall History

Side Effects Reported to FDA

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

chest pain2 reports
chronic kidney disease2 reports
fall2 reports
respiratory syncytial virus infection2 reports
acute kidney injury1 reports
adverse drug reaction1 reports
aggression1 reports
arthralgia1 reports
atypical pneumonia1 reports
balance disorder1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses temporarily relieves these symptoms due to the common cold, hay fever, (allergic rhinitis) or other upper respiratory allergies: runny nose sneezing itching of nose or throat itchy, watery eyes cough due to minor throat and bronchial irritation nasal congestion reduces swelling of nasal passages

Dosage & Administration

Directions Do not exceed recommended dosage. Adults and children 12 years of age and older: 4 teaspoonfuls (20 mL) every 4 hours, not to exceed 24 teaspoonfuls in 24 hours. Children 6 to under 12 years of age: 2 teaspoonfuls (10 mL) every 4 hours, not to exceed 12 teaspoonfuls in 24 hours. Children under 6 years of age: Consult a doctor

Warnings

Warnings Do not exceed recommended dosage. Do not use this product 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 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 a breathing problem such as emphysema or chronic bronchitis glaucoma trouble urinating to to an enlarged prostate gland a cough that lasts or is chronic such as occurs with smoking, asthma or emphysema a cough that occurs with too much phlegm (mucus) heart disease high blood pressure thyroid disease diabetes Ask a doctor or pharmacist before use if you are taking sedatives or tranquilizers. When using this product excitability may occur, especially in children may cause marked drowsiness avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase the drowsiness effect be careful when driving a motor vehicle or operating machinery Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur cough or nasal congestion persists for m

Frequently Asked Questions

What is Rynex DM used for?

Rynex DM contains Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride. It is a liquid taken oral. Consult your doctor for specific uses.

Is Rynex DM a controlled substance?

Rynex DM is not classified as a controlled substance by the DEA.

What is the generic name for Rynex DM?

The generic name for Rynex DM is Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride. There are 3 other brand versions of Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride.

What is the NDC code for Rynex DM 1 mg/5mL?

The NDC (National Drug Code) for Rynex DM 1 mg/5mL is 0485-0204, listed by Edwards Pharmaceuticals, Inc.

Product NDC

0485-0204

Package NDC

0485-0204-04

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

Data from openFDA · Public domain (CC0 1.0)