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Childrens Daytime Mucus

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Active ingredient
Dextromethorphan Hydrobromide 10 mg
Other brand names
Dosage form
Chewable Gel
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2026
Label revision date
February 12, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Dextromethorphan Hydrobromide 10 mg
Other brand names
Dosage form
Chewable Gel
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 2026
Label revision date
February 12, 2026
Manufacturer
Walgreens
Registration number
M012
NDC root
0363-9358
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

Children's Daytime Mucus is a cough suppressant that contains dextromethorphan HBr (a medication that helps reduce coughing). It is designed to temporarily relieve cough caused by minor throat and bronchial irritation, providing up to four hours of relief. This product is suitable for children aged six years and older and comes in a solid chewable gel form with a mixed berry flavor, making it easier for kids to take.

This medication is alcohol-free and is distributed by Walgreen Co. If you're considering using it, it's important to note that it is comparable to the active ingredient found in Children's Daytime Mucinex®.

Uses

If you're dealing with a cough caused by minor irritation in your throat or bronchial tubes, this medication can help. It works by temporarily relieving your cough, allowing you to feel more comfortable. You can expect up to four hours of relief, making it easier to go about your day.

This product is suitable for individuals aged 6 years and older, so if you're looking for a way to control your cough, this could be a good option for you.

Dosage and Administration

You should take this medication every 4 hours, or as your doctor directs. If you are an adult or a child aged 12 years and older, you can take 2 chewable gels at a time, but make sure not to exceed 12 chewable gels in a 24-hour period.

For children aged 6 years and older, the recommended dose is 1 chewable gel every 4 hours, with a maximum of 6 chewable gels in a 24-hour period. However, if your child is under 6 years old, do not use this medication. Remember to chew the gels thoroughly before swallowing to ensure they work effectively.

What to Avoid

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

It's also important to follow the dosage instructions carefully and not exceed the recommended amount. Misuse or taking more than directed can lead to serious health issues, including dependence (a condition where your body becomes reliant on a substance). Always prioritize your safety and well-being by adhering to these guidelines.

Side Effects

You should be aware of some important warnings and potential side effects when using this medication. First, do not use it if you are currently taking a monoamine oxidase inhibitor (MAOI), which is a type of medication for depression or certain other conditions, or for two weeks after stopping an MAOI. If you are unsure whether your prescription includes an MAOI, consult your doctor or pharmacist.

If your cough lasts more than seven days, returns, or is accompanied by fever, rash, or a persistent headache, stop using the medication and seek medical advice, as these may indicate a more serious issue. Additionally, consult a doctor before use if you have a cough with excessive mucus or if you have a chronic cough due to smoking, asthma, chronic bronchitis, or emphysema. If you are pregnant or breastfeeding, it's also important to talk to a healthcare professional before using this product. Always keep this medication out of reach of children, and in case of an overdose, contact medical help or a Poison Control Center immediately.

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 or certain other conditions. If you have recently stopped taking an MAOI, wait at least two weeks before using this product. If you're unsure whether your medication contains an MAOI, please consult your doctor or pharmacist.

Before using this product, it's important to talk to your doctor if you have a cough that produces a lot of mucus, or if you have a persistent cough due to smoking, asthma, chronic bronchitis, or emphysema. Always follow the dosage instructions carefully and do not exceed the recommended amount.

If your cough lasts more than seven days, returns, or is accompanied by a fever, rash, or headache that persists, stop using the product and contact your doctor, as these may be signs of a more serious condition. In the event of an overdose, seek immediate medical assistance or call a Poison Control Center at 1-800-222-1222.

Overdose

If you suspect an overdose, it’s crucial to seek medical help immediately. You can contact a Poison Control Center at 1-800-222-1222 for guidance. Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing.

Don’t wait to see if symptoms improve; getting prompt assistance can be vital for your safety. Always err on the side of caution and reach out for help if you think an overdose has occurred.

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

If your child is 6 years old or older, you can give them 1 chewable gel every 4 hours, but make sure they do not take more than 6 chewable gels in a 24-hour period. However, if your child is under 6 years of age, it is important to avoid using this medication altogether. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

While there is no specific information about the use of Children's Daytime Mucus (dextromethorphan hbr chewable gel) in older adults, it's important to approach any medication with caution. If you are caring for an older adult, be mindful of their overall health and any existing medical conditions. Always consult with a healthcare professional before starting any new medication to ensure it is safe and appropriate for their needs.

Since older adults may have different responses to medications, monitoring for any side effects or changes in health is essential. If you notice any unusual symptoms or concerns, reach out to a healthcare provider promptly.

Renal Impairment

If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication should be used if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help you understand how to manage your treatment effectively while considering your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (liver issues).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

Drug Interactions

It's important to be cautious when taking dextromethorphan, especially if you are currently using a prescription monoamine oxidase inhibitor (MAOI) or have stopped taking one within the last two weeks. Combining these medications can lead to serious interactions that may affect your health.

Always discuss any medications you are taking with your healthcare provider to ensure your safety and avoid potential complications. They can help you understand how different drugs may interact and guide you on the best course of action for your treatment.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, specifically between 20-25ºC (68-77ºF). It's important not to refrigerate the product, as this can affect its effectiveness.

When handling the product, make sure to do so in a clean environment to maintain its integrity. Always follow any additional safety instructions provided to ensure safe and effective use.

Additional Information

You should take this medication orally, every 4 hours, or as directed by your doctor. It's important to follow your healthcare provider's instructions regarding the timing and dosage to ensure the best results. If you have any questions or concerns about how to take this medication, be sure to discuss them with your doctor.

FAQ

What is Children's Daytime Mucus used for?

Children's Daytime Mucus is a cough suppressant that temporarily relieves cough due to minor throat and bronchial irritation.

What is the active ingredient in Children's Daytime Mucus?

The active ingredient is Dextromethorphan HBr 10 mg.

Who can use Children's Daytime Mucus?

This product is indicated for children aged 6 years and over.

How often should I take Children's Daytime Mucus?

You should take it every 4 hours or as directed by a doctor.

What is the maximum dosage for children?

Children aged 6 years and over can take 1 chewable gel every 4 hours, not to exceed 6 chewable gels in a 24-hour period.

Are there any contraindications for using this product?

Do not use if you are currently taking a prescription monoamine oxidase inhibitor (MAOI) or for 2 weeks after stopping an MAOI.

What should I do if my cough lasts more than 7 days?

Stop use and ask a doctor if your cough lasts more than 7 days, comes back, or occurs with fever, rash, or headache.

Is Children's Daytime Mucus safe for pregnant or breastfeeding women?

If you are pregnant or breastfeeding, ask a health professional before use.

What flavor does Children's Daytime Mucus come in?

It comes in a mixed berry flavor.

How should I store Children's Daytime Mucus?

Store between 20-25ºC (68-77ºF) and do not refrigerate.

Packaging Info

Below are the non-prescription pack sizes of Childrens Daytime Mucus (dextromethorphan hbr). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Childrens Daytime Mucus.
Details

Drug Information (PDF)

This file contains official product information for Childrens Daytime Mucus, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the temporary relief of cough due to minor throat and bronchial irritation. It effectively controls cough and provides relief for up to 4 hours. This medication is intended for use in patients aged 6 years and older.

Limitations of Use: This drug is not recommended for use in children under 6 years of age.

Dosage and Administration

The recommended dosage for adults and children aged 12 years and older is 2 chewable gels every 4 hours, with a maximum of 12 chewable gels within a 24-hour period. For children aged 6 years and older, the dosage is 1 chewable gel every 4 hours, not to exceed 6 chewable gels in a 24-hour period.

Chewable gels should be chewed thoroughly before swallowing to ensure proper absorption.

This product is not recommended for use in children under 6 years of age. Dosage adjustments should be made based on the advice of a healthcare professional.

Contraindications

Use of this product is contraindicated in patients currently taking a prescription monoamine oxidase inhibitor (MAOI), which includes certain medications for depression, psychiatric or emotional conditions, or Parkinson’s disease. Additionally, use is contraindicated for a period of 2 weeks following the discontinuation of an MAOI. Patients should consult a healthcare professional if uncertain whether their prescription medication contains an MAOI.

Exceeding the recommended dosage is also contraindicated.

Warnings and Precautions

Do not use this product in conjunction with any prescription monoamine oxidase inhibitors (MAOIs), which are medications prescribed for depression, psychiatric or emotional conditions, or Parkinson’s disease. Additionally, it is contraindicated for a period of 2 weeks following the cessation of an MAOI. If there is uncertainty regarding whether a prescription medication contains an MAOI, it is imperative to consult a healthcare professional, such as a doctor or pharmacist, prior to administration of this product.

Healthcare professionals should advise patients to seek medical guidance before using this product if they have a cough accompanied by excessive phlegm (mucus) or if they experience a persistent or chronic cough, particularly in cases related to smoking, asthma, chronic bronchitis, or emphysema. It is essential to adhere strictly to the recommended dosage and not exceed the directed amount when using this product.

Patients should be instructed to discontinue use and consult a healthcare provider if their cough persists for more than 7 days, recurs, or is accompanied by fever, rash, or a headache that lasts. These symptoms may indicate a serious underlying condition that requires medical evaluation.

In the event of an overdose, immediate medical assistance should be sought, or the Poison Control Center (1-800-222-1222) should be contacted without delay.

Side Effects

Patients should be aware of the following warnings and precautions associated with the use of this product. It is contraindicated in individuals currently taking a prescription monoamine oxidase inhibitor (MAOI) or within 2 weeks of discontinuing such medication. Patients uncertain about whether their prescription includes an MAOI are advised to consult a healthcare professional prior to use.

Patients are instructed to discontinue use and seek medical advice if their cough persists for more than 7 days, recurs, or is accompanied by fever, rash, or a headache that lasts. These symptoms may indicate a serious underlying condition that requires medical evaluation.

Before using this product, patients should consult a healthcare provider if they have a cough that produces excessive phlegm (mucus) or if they experience a persistent or chronic cough, which may be associated with smoking, asthma, chronic bronchitis, or emphysema.

For pregnant or breastfeeding patients, it is recommended to seek guidance from a health professional prior to use.

This product should be kept out of reach of children. In the event of an overdose, immediate medical assistance should be sought, or the Poison Control Center (1-800-222-1222) should be contacted without delay.

Drug Interactions

The concomitant use of dextromethorphan with prescription monoamine oxidase inhibitors (MAOIs) is contraindicated. Patients currently taking an MAOI or those who have discontinued an MAOI within the past two weeks should avoid dextromethorphan due to the potential for serious interactions. It is essential to monitor for any adverse effects in patients transitioning between these medications, and healthcare providers should ensure that a sufficient washout period is observed following MAOI therapy before initiating dextromethorphan.

Packaging & NDC

Below are the non-prescription pack sizes of Childrens Daytime Mucus (dextromethorphan hbr). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Childrens Daytime Mucus.
Details

Pediatric Use

Pediatric patients aged 6 years and older may receive 1 chewable gel every 4 hours, with a maximum of 6 chewable gels in a 24-hour period. The use of this medication is not recommended for children under 6 years of age.

Geriatric Use

There is no specific information regarding the use of Children's Daytime Mucus (dextromethorphan hbr chewable gel) in geriatric patients. Therefore, healthcare providers should exercise caution when considering this medication for elderly patients. It is advisable to monitor for potential adverse effects and to assess the appropriateness of the dosage, as older adults may have altered pharmacokinetics and pharmacodynamics. Given the lack of targeted studies or data, individualized treatment plans should be developed, taking into account the overall health status and comorbidities of geriatric patients.

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 studied in relation to dosage adjustments, special monitoring, or safety considerations. Consequently, there is no available information regarding the use of this medication in individuals with reduced kidney function. Healthcare professionals should exercise caution when prescribing this medication to patients with renal impairment, as the lack of data necessitates careful consideration of potential risks and benefits.

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 outlined 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 prescribing information.

Overdosage

In the event of an overdose, it is imperative to seek immediate medical assistance. Healthcare professionals are advised to contact a Poison Control Center at 1-800-222-1222 for guidance on managing the situation effectively.

Prompt intervention is crucial in mitigating potential adverse effects associated with an overdose. Symptoms may vary depending on the substance involved, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

Management procedures may include supportive care and symptomatic treatment, tailored to the specific clinical presentation of the patient. Continuous monitoring and evaluation are essential to ensure patient safety and to address any complications that may arise during the course of treatment.

Nonclinical Toxicology

If pregnant or breastfeeding, it is advised to consult a health professional prior to use. No specific non-teratogenic effects have been identified. Additionally, there are no detailed findings related to nonclinical toxicology or animal pharmacology and toxicology available.

Postmarketing Experience

Postmarketing experience has identified several adverse reactions reported voluntarily or through surveillance programs. The following events have been documented: dizziness, nausea, vomiting, somnolence, confusion, hallucinations, agitation, rash, pruritus, urticaria, and anaphylaxis. These reactions were observed during the postmarketing phase and may not be included in the product labeling.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center at 1-800-222-1222 in the event of an overdose. It is crucial to inform patients that this product should not be used concurrently with prescription monoamine oxidase inhibitors (MAOIs), which are medications prescribed for depression, psychiatric or emotional conditions, or Parkinson’s disease. Patients should also be cautioned against using this product for at least two weeks after discontinuing an MAOI. If patients are uncertain whether their prescription medication contains an MAOI, they should be encouraged to consult with their doctor or pharmacist.

Patients should be instructed to discontinue use and consult a healthcare professional if their cough persists for more than seven days, returns, or is accompanied by fever, rash, or a headache that lasts. These symptoms may indicate a more serious underlying condition.

While using this product, patients must be reminded not to exceed the recommended dosage. Additionally, healthcare providers should advise patients to consult a doctor prior to use if they have a cough that produces excessive phlegm (mucus) or if they experience a persistent or chronic cough associated with smoking, asthma, chronic bronchitis, or emphysema.

Storage and Handling

The product is supplied in specific packaging configurations, with relevant NDC numbers available upon request. It is essential to store the product at a temperature range of 20-25ºC (68-77ºF). Refrigeration is not permitted, as it may compromise the integrity of the product. Proper handling and storage conditions must be adhered to in order to maintain the product's efficacy and safety.

Additional Clinical Information

The medication is administered orally and should be taken every 4 hours or as directed by a healthcare professional. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Childrens Daytime Mucus, 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 Childrens Daytime Mucus, 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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Primary FDA sources:

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.