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Guaifenesin dm - Medication Information

Product NDC Code 60687-817
Drug Name

Guaifenesin dm

Type Brand
Pharm Class Decreased Respiratory Secretion Viscosity [PE],
Expectorant [EPC],
Increased Respiratory Secretions [PE],
Sigma-1 Agonist [EPC],
Sigma-1 Receptor Agonists [MoA],
Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC],
Uncompetitive NMDA Receptor Antagonists [MoA]
Active Ingredients
Dextromethorphan 10 mg/5ml
Guaifenesin 100 mg/5ml
Route ORAL
Dosage Form SYRUP
RxCUI drug identifier 996520
Application Number M012
Labeler Name American Health Packaging
Packages
Package NDC Code Description
60687-817-17 10 tray in 1 case (60687-817-17) / 10 cup, unit-dose in 1 tray (60687-817-46) / 5 ml in 1 cup, unit-dose (60687-817-40)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each 5 mL Cup) Guaifenesin 100 mg Dextromethorphan Hydrobromide 10 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Follow dosage below or use as directed by a physician. do not take more than 6 doses in any 24-hour period. Age (yr) Dose (mL) adults and children 12 years and over 10 mL (2 teaspoonfuls) every 4 hours children 6 years to under 12 years 5 mL (1 teaspoonful) every 4 hours children 2 years to under 6 years 2.5 mL (1/2 teaspoonful) every 4 hours children under 2 years ask a doctor
Age (yr)Dose (mL)
adults and children 12 years and over10 mL (2 teaspoonfuls) every 4 hours
children 6 years to under 12 years5 mL (1 teaspoonful) every 4 hours
children 2 years to under 6 years2.5 mL (1/2 teaspoonful) every 4 hours
children under 2 yearsask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients citric acid, FD&C Red No. 40, flavoring, glycerin, menthol, purified water, sodium benzoate, sodium citrate, sodium saccharin, and sucrose.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses helps loosen phlegm (mucus) and thin bronchial secretions to make coughs more productive temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold

Purpose

Information about the drug product’s indications for use.
Purpose Expectorant Cough Suppressant

Spl product data elements

Usually a list of ingredients in a drug product.
Guaifenesin DM Guaifenesin and Dextromethorphan ANHYDROUS CITRIC ACID FD&C RED NO. 40 GLYCERIN MENTHOL, UNSPECIFIED FORM WATER SODIUM BENZOATE SODIUM CITRATE, UNSPECIFIED FORM SACCHARIN SODIUM SUCROSE GUAIFENESIN GUAIFENESIN DEXTROMETHORPHAN DEXTROMETHORPHAN DEXTROMETHORPHAN HYDROBROMIDE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package/Label Principal Display Panel - Label Case NDC 60687-817-17/Cup NDC 60687-817-40 GUAIFENESIN and DEXTROMETHORPHAN SYRUP Expectorant/Cough Suppressant 100 mg/10 mg per 5 mL Non-Narcotic, Alcohol Free Cherry Flavor Usual Dosage: See attached Drug Facts. Store at 20° to 25°C (68° to 77°F) [See USP] Protect from light. FOR INSTITUTIONAL USE ONLY T0638C050324 R03/24 GUAIFENESIN and DEXTROMETHORPHAN SYRUP Label Package/Label Principal Display Panel – Cup Lid – 100 mg/10 mg per 5 mL NDC 60687- 817 -40 Guaifenesin and Dextromethorphan Syrup Expectorant/cough Suppressant 100 mg/10 mg per 5 mL Delivers 5 mL Protect from light See package Drug Facts insert for full prescribing information and storage For Institutional Use Only. American Health Packaging Columbus, OH 43217 F0638C050224 GUAIFENESIN and DEXTROMETHORPHAN SYRUP Cup Lid

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Professional Note: Guaifenesin has been shown to produce a color interference with certain clinical laboratory determinations of 5-hydroxyindoleacetic acid (5-HIAA) and vanillylmandelic acid (VMA). Distributed by: American Health Packaging Columbus, OH 43217 R0324

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
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

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other Information Each 5 mL contains: sodium 4 mg Store at controlled room temperature between 20° to 25°C (68° to 77°F) [see USP]. Protect from light. DO NOT USE IF SEAL IS BROKEN. Guaifenesin Syrup and Dextromethorphan is a red, cherry flavored syrup and is available in the following dosage forms: 5 mL unit-dose cups: 100 cups (10 x 10) NDC 60687-817-17 10 mL unit-dose cups: 100 cups (10 x 10) NDC 60687-828-56

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? Call 1-800-845-8210

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
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. you are hypersensitive to any of the ingredients.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional before use.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 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. you are hypersensitive to any of the ingredients. 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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API