VANACOF DM 18 mg/15mL

DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE · LIQUID · GM Pharmaceuticals, INC

No Recall History

Plain English

VANACOF DM is a liquid containing dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride at 18 mg/15mL, taken oral. Manufactured by GM Pharmaceuticals, INC.

Key Facts

Brand Name: VANACOF DM
Generic Name: DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
NDC Code (Product): 58809-555
Manufacturer: GM Pharmaceuticals, INC
Strength: 18 mg/15mL
Dosage Form: LIQUID
Route: ORAL
Marketing Status
Application #: M012
Drug Class: Expectorant [EPC]
Marketing Start: 06/01/2013

Recall History

No Recall History

Side Effects Reported to FDA

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

cataplexy1 reports

hypersensitivity1 reports

pharyngitis1 reports

sinusitis1 reports

tenon^s capsule thickening1 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep nasal congestion due to a cold

Dosage & Administration

Directions do not take more than 6 doses in any 24-hour period use enclosed dosage cup or tablespoon (TBSP) dose as follows or as directed by a doctor Adults and children 12 years of age and over: 15 mL (1 TBSP) every 4 hours, not to exceed 90 mL (6 TBSP) in a 24 hour period. Children 6 to under 12 years of age: 7.5 mL (1/2 TBSP) every 4 hours, not to exceed 45 mL (3 TBSP) in a 24 hour period. Children under 6 years of age: Consult a doctor.

Warnings

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 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 heart disease high blood pressure thyroid disease diabetes a cough that lasts or is chronic such as occurs with smoking, asthma, or emphysema a cough that occurs with too much phlegm (mucus) difficulty in urination due to enlargement of the prostate gland When using this product do not use more than directed Stop use and ask a doctor if: nervousness, dizziness or sleeplessness occurs symptoms do not improve within 7 days or are accompanied by a fever, rash or persistent headache. A persistant cough may be a sign of a serious condition. new symptoms occur 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 VANACOF DM used for?

VANACOF DM contains DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE. It is a liquid taken oral. Consult your doctor for specific uses.

Is VANACOF DM a controlled substance?

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

What is the generic name for VANACOF DM?

The generic name for VANACOF DM is DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE. There are 11 other brand versions of DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE.

What is the NDC code for VANACOF DM 18 mg/15mL?

The NDC (National Drug Code) for VANACOF DM 18 mg/15mL is 58809-555, listed by GM Pharmaceuticals, INC.

Product NDC

58809-555

Package NDC

58809-555-08

Other Dextromethorphan Brands

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

Data from openFDA · Public domain (CC0 1.0)