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Revasol Tussin Dm Max with Honey

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Active ingredients
  • Guaifenesin 400 mg/20 mL
  • Dextromethorphan Hydrobromide 20 mg/20 mL
Other brand names
Drug classes
Expectorant, Sigma-1 Agonist, Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Dosage form
Liquid
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
March 21, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Guaifenesin 400 mg/20 mL
  • Dextromethorphan Hydrobromide 20 mg/20 mL
Other brand names
Drug classes
Expectorant, Sigma-1 Agonist, Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Dosage form
Liquid
Route
Oral
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
March 21, 2025
Manufacturer
Rnv LLC
Registration number
M012
NDC root
84379-274
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

REVASOL DM MAX HONEY is a medication designed to temporarily relieve coughs that may occur with the common cold. It works by loosening phlegm (mucus) and thinning bronchial secretions, which helps clear out bothersome mucus from your airways. This can make it easier for you to breathe and feel more comfortable when you're dealing with a cough associated with a cold.

Uses

You can use this medication to temporarily relieve a cough that often comes with the common cold. It also helps to loosen phlegm (mucus) and thin out bronchial secretions, making it easier for you to clear out bothersome mucus from your airways. This can provide some comfort when you're feeling under the weather.

Dosage and Administration

Before using this medication, make sure to shake the bottle well. You should measure your dose using the dosing cup that comes with the product, as this ensures you get the correct amount. For adults and children aged 12 years and older, the recommended dose is 20 milliliters (mL) every 4 hours. However, it's important not to take more than 6 doses within a 24-hour period.

Please remember that this product is specifically designed for adults and is not suitable for children under 12 years of age. Always keep the dosing cup with the product to avoid any confusion when measuring your dose.

What to Avoid

It's important to keep this medication out of the reach of children to ensure their safety. If your cough lasts more than a week, comes back frequently, or is accompanied by symptoms like fever, rash, or a persistent headache, you should stop using the medication and consult your doctor. This will help ensure that you receive the appropriate care and guidance for your health.

Side Effects

You should be aware of some important side effects and warnings associated with this medication. If you are currently taking a prescription monoamine oxidase inhibitor (MAOI) for conditions like depression or Parkinson’s disease, or if you have stopped taking one within the last two weeks, do not use this product. It's essential to consult your doctor or pharmacist if you're unsure whether your medication contains an MAOI.

If your cough lasts more than a week, keeps coming back, or is accompanied by symptoms like fever, rash, or a persistent headache, you should stop using the medication and seek medical advice, as these could indicate a more serious condition. Additionally, consult your doctor before using this product if you have a cough with excessive mucus or if you have a chronic cough related to smoking, asthma, chronic bronchitis, or emphysema.

Warnings and Precautions

You should not use this product if you are currently taking a prescription monoamine oxidase inhibitor (MAOI), which is a type of medication used for depression, certain psychiatric conditions, or Parkinson’s disease. Additionally, you must wait at least two weeks after stopping an MAOI before using this product. If you are unsure whether your medication contains an MAOI, please consult your doctor or pharmacist.

In case of an accidental overdose, it is crucial to seek emergency medical help or contact a Poison Control Center immediately. You should also stop using this product and call your doctor if your cough lasts more than one week, keeps coming back, or is accompanied by a fever, rash, or persistent headache, as these could be signs of a more serious health issue.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

This product is designed specifically for adults and is not suitable for children. If your child is under 12 years old, it is important to avoid using this medication. Always consult with a healthcare professional if you have questions about appropriate treatments for your child.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always wise to discuss any medications with a healthcare provider, especially considering factors like kidney function and changes in cognition (thinking and memory) that can occur with age.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health needs and conditions. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

Renal Impairment

If you have kidney issues, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that there are no special monitoring requirements or safety considerations outlined for patients with renal impairment (kidney problems).

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can provide guidance tailored to your specific situation.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may want to conduct regular liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

Drug Interactions

It's crucial to be aware of potential interactions when taking medications. If you are currently using a prescription monoamine oxidase inhibitor (MAOI), which is a type of medication often prescribed for depression, psychiatric conditions, or Parkinson’s disease, you should not take this product. Additionally, you should wait at least two weeks after stopping an MAOI before starting this medication. If you're unsure whether your current prescription includes an MAOI, please consult your doctor or pharmacist for clarification.

Always discuss any medications you are taking with your healthcare provider to ensure your safety and avoid harmful interactions. Your health is important, and your provider can help you make informed decisions about your treatment.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, specifically between 15-30°C (59-86°F). It's important not to refrigerate the product, as this could affect its effectiveness.

When handling the product, always do so with clean hands and in a clean environment to maintain safety and prevent contamination. Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is REVASOL DM MAX HONEY used for?

REVASOL DM MAX HONEY temporarily relieves cough associated with the common cold and helps loosen phlegm (mucus) and thin bronchial secretions.

What is the recommended dosage for adults?

Adults and children 12 years of age and over should take 20 mL every 4 hours, not exceeding 6 doses in any 24-hour period.

Is this product safe for children?

No, this adult product is not intended for use in children under 12 years of age.

What should I do if my cough persists?

Stop use and ask a doctor if your cough persists for more than 1 week, tends to recur, or is accompanied by a fever, rash, or persistent headache.

Are there any contraindications for using this product?

Do not use REVASOL DM MAX HONEY if you are currently taking a prescription monoamine oxidase inhibitor (MAOI) or have taken one within the last 2 weeks.

What should I do in case of an accidental overdose?

In case of accidental overdose, get medical help or contact a Poison Control Center immediately.

Can I use this product if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before using REVASOL DM MAX HONEY.

How should I store REVASOL DM MAX HONEY?

Store REVASOL DM MAX HONEY at room temperature between 15-30°C (59-86°F) and do not refrigerate.

Packaging Info

Below are the non-prescription pack sizes of Revasol Tussin Dm Max with Honey (dextromethorphan hbr and guaifenesin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Revasol Tussin Dm Max with Honey.
Details

Drug Information (PDF)

This file contains official product information for Revasol Tussin Dm Max with Honey, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

REVASOL DM MAX is a pharmaceutical formulation that combines Dextromethorphan HBr, Guaifenesin, and Phenylephrine HCl. Dextromethorphan HBr is characterized as a white to off-white crystalline powder, exhibiting solubility in both water and alcohol. Guaifenesin is also a white crystalline powder, which is soluble in water. Phenylephrine HCl appears as a white to off-white crystalline powder, similarly soluble in water.

The formulation includes several inactive ingredients: citric acid, sodium citrate, sucrose, natural and artificial flavors, sodium benzoate, and water. REVASOL DM MAX is presented in a honey-flavored syrup dosage form.

Uses and Indications

This drug is indicated for the temporary relief of cough associated with the common cold. It also aids in loosening phlegm (mucus) and thinning bronchial secretions, facilitating the clearance of bothersome mucus from the bronchial passageways.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The recommended dosage for adults and children aged 12 years and older is 20 mL administered every 4 hours as needed. It is imperative that no more than 6 doses are taken within a 24-hour period.

Prior to administration, the product must be shaken well to ensure proper mixing. The dosing should be measured exclusively with the dosing cup provided, which should be kept with the product at all times.

This formulation is specifically designed for adult use and is not intended for children under 12 years of age.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. Additionally, if cough persists for more than one week, tends to recur, or is accompanied by fever, rash, or persistent headache, discontinue use and consult a healthcare professional.

Warnings and Precautions

It is imperative that this product not be used concurrently with prescription monoamine oxidase inhibitors (MAOIs), which are medications prescribed for depression, psychiatric disorders, emotional conditions, or Parkinson’s disease. Additionally, this product should not be taken for a minimum of two weeks following the discontinuation of an MAOI. Healthcare professionals should advise patients to consult with a doctor or pharmacist if there is uncertainty regarding the presence of an MAOI in their current prescription medications.

In the event of an accidental overdose, immediate medical assistance should be sought. Patients or caregivers are encouraged to contact a Poison Control Center without delay to ensure appropriate management of the situation.

Patients should be instructed to discontinue use of this product and consult their healthcare provider if a cough persists for more than one week, recurs, or is accompanied by additional symptoms such as fever, rash, or a persistent headache. A persistent cough may indicate an underlying serious condition that requires further evaluation and intervention.

Side Effects

Patients should be aware of the potential adverse reactions associated with the use of this product. Serious adverse reactions may occur, particularly in patients who are currently taking or have recently discontinued a prescription monoamine oxidase inhibitor (MAOI). The use of this product is contraindicated in such cases, and patients are advised to consult a healthcare professional if they are uncertain whether their prescription medication contains an MAOI.

Common adverse reactions may include a persistent cough that lasts more than one week, recurs, or is accompanied by additional symptoms such as fever, rash, or persistent headache. These symptoms may indicate a serious underlying condition, and patients should discontinue use and seek medical advice if they experience these signs.

Additionally, patients should consult a healthcare provider before using this product if they have a cough that is accompanied by excessive phlegm (mucus) or if they suffer from a persistent or chronic cough, which may be associated with conditions such as smoking, asthma, chronic bronchitis, or emphysema.

Drug Interactions

The concomitant use of this product with prescription monoamine oxidase inhibitors (MAOIs) is contraindicated. MAOIs are typically prescribed for the treatment of depression, certain psychiatric conditions, or Parkinson’s disease. Patients should not take this product while on MAOIs or within 2 weeks of discontinuing an MAOI. It is essential for patients to consult with a healthcare professional, such as a doctor or pharmacist, to verify whether their current prescription includes an MAOI before initiating treatment with this product.

Packaging & NDC

Below are the non-prescription pack sizes of Revasol Tussin Dm Max with Honey (dextromethorphan hbr and guaifenesin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Revasol Tussin Dm Max with Honey.
Details

Pediatric Use

This product is not intended for use in pediatric patients. Specifically, it is contraindicated in children under 12 years of age. Healthcare professionals should exercise caution and refrain from prescribing this medication to this age group.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as they may have altered pharmacokinetics and pharmacodynamics. Close monitoring is recommended to ensure safety and efficacy in this population.

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is no specific data available regarding the excretion of this medication in breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating individuals.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of information necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this medication. Consequently, there are no established dosage adjustments, special monitoring requirements, or precautions for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be prudent in these cases, although specific parameters are not defined in the available information.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the substance involved, estimated dose, and time of exposure, is crucial for effective management and follow-up care.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of the reach of children. In the event of an accidental overdose, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be instructed to stop using the medication and consult a doctor if their cough persists for more than one week, tends to recur, or is accompanied by symptoms such as fever, rash, or a persistent headache. It is important to inform patients that a persistent cough may indicate a serious underlying condition.

Additionally, healthcare providers should recommend that patients consult a doctor before using the medication if they have a cough that is accompanied by excessive phlegm (mucus) or if they experience a persistent or chronic cough, which may occur with conditions such as smoking, asthma, chronic bronchitis, or emphysema.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at room temperature, maintaining a range of 15-30°C (59-86°F). Refrigeration is not permitted, as it may compromise the integrity of the product. Proper handling should be observed to ensure optimal quality and efficacy.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Revasol Tussin Dm Max with Honey, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Revasol Tussin Dm Max with Honey, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

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Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.