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Drx Choice Children Daytime

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Active ingredients
  • Guaifenesin 200 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)
Marketed in the U.S.
Since 2023
Label revision date
September 29, 2025
Active ingredients
  • Guaifenesin 200 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
Marketed in the U.S.
Since 2023
Label revision date
September 29, 2025
Manufacturer
RARITAN PHARMACEUTICALS
Registration number
M012
NDC root
68163-747

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

Drug Overview

DRx Choice Children's Daytime Cough & Chest Congestion is a medication designed to temporarily relieve cough caused by minor throat and bronchial irritation, which can occur with a cold. It works by helping to loosen phlegm (mucus) and thin bronchial secretions, making it easier to drain the bronchial tubes.

This product contains two active ingredients: Dextromethorphan HBr, which acts as a cough suppressant, and Guaifenesin, an expectorant that helps clear mucus from the airways. It is sugar-free, dye-free, and alcohol-free, making it suitable for children aged 4 and over. The medication is available in a pleasant grape flavor, ensuring that it is more enjoyable for kids to take.

Uses

If you're dealing with a cough caused by minor irritation in your throat or bronchial tubes, especially during a cold, this medication can provide temporary relief. It works by soothing your throat and helping to ease the discomfort associated with coughing.

Additionally, this medication helps to loosen phlegm (mucus) and thin out bronchial secretions, making it easier for your body to clear out mucus from your airways. This can be particularly helpful if you're feeling congested or have difficulty breathing due to mucus buildup.

Dosage and Administration

When using this medication, it's important to follow the dosing guidelines carefully to ensure safety and effectiveness. You should never take more than 6 doses within a 24-hour period. To measure your dose accurately, always use the dosing cup that comes with the product, and keep it handy for each use.

For children, the dosage varies by age. If your child is under 4 years old, do not use this medication. For children aged 4 to under 6 years, the recommended dose is 5 milliliters (mL) every 4 hours. If your child is between 6 and under 12 years, they should take 10 mL every 4 hours. For adults and children aged 12 years and older, the dose is 20 mL every 4 hours. Always ensure you are measuring the correct amount to keep everyone safe.

What to Avoid

You should avoid using this product if you are currently taking a prescription monoamine oxidase inhibitor (MAOI), which is a type of medication used for depression, psychiatric, or emotional conditions, or Parkinson's disease. Additionally, do not use this product for at least two weeks after stopping an MAOI. If you're unsure whether your child's prescription includes an MAOI, it's important to consult with a doctor or pharmacist before using this product.

Taking this medication while on an MAOI can lead to serious health risks, so please prioritize your safety by following these guidelines closely.

Side Effects

If you experience a cough that lasts more than 7 days, returns after disappearing, or is accompanied by symptoms like fever, rash, or a persistent headache, it could indicate a serious condition, and you should seek medical attention. Additionally, be aware that a cough with excessive phlegm (mucus) or a chronic cough related to smoking, asthma, chronic bronchitis, or emphysema may also require further evaluation.

Warnings and Precautions

If you are taking a prescription monoamine oxidase inhibitor (MAOI) for depression, psychiatric conditions, or Parkinson's disease, do not use this product. You should also wait at least two weeks after stopping an MAOI before using it. If you're unsure whether your child's medication contains an MAOI, please consult a doctor or pharmacist.

It's important to stop using this product and contact your doctor if your cough lasts more than seven days, returns, or is accompanied by a fever, rash, or persistent headache, as these may indicate a more serious issue. In case of an overdose, seek medical help immediately or call the Poison Control Center at 1-800-222-1222.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the potential signs of an overdose, which can include unusual drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, contact your local poison control center or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any risk of overdose. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

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 you are considering this medication for your child, it's important to know the age guidelines. This product is not recommended for children under 4 years old. For children aged 4 to under 6 years, the appropriate dosage is 5 mL every 4 hours. If your child is between 6 and 12 years old, they can take 10 mL every 4 hours.

For anyone aged 12 and older, including adults, the dosage increases to 20 mL every 4 hours. Always ensure you follow these guidelines to keep your child safe and healthy.

Geriatric Use

While there is no specific information about the use of this medication in older adults, it’s important to remember that each person’s health needs can vary. Since the insert does not mention any age-related dosage adjustments, safety concerns, or special precautions for elderly patients, you should always consult with a healthcare provider before starting any new medication. They can help ensure that the treatment is appropriate for your individual health situation and any other medications you may be taking.

Renal Impairment

If you have kidney problems, it's important to know that you may need a lower dose of this medication. Your doctor will determine the right dosage based on your creatinine clearance, which is a test that measures how well your kidneys are filtering waste from your blood.

To ensure your kidneys remain healthy while taking this medication, regular renal function tests are recommended. If you have severe kidney impairment, your healthcare provider will need to monitor you more closely to adjust your treatment as necessary. Always discuss any concerns with your doctor to ensure your safety and well-being.

Hepatic Impairment

If you have liver problems, it's important to know that your condition can affect how your body processes certain medications. This means that you may need to adjust your dosage to ensure the drug works effectively and safely.

For those with severe liver impairment, a lower dose or a different treatment option might be necessary. Additionally, your healthcare provider will likely recommend regular monitoring of your liver function tests (which check how well your liver is working) to keep track of your health while on medication. Always discuss any concerns with your doctor to ensure the best care for your situation.

Drug Interactions

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

Always discuss any medications you are taking with your healthcare provider. They can help ensure that your treatments are safe and effective, and they can provide guidance on any potential interactions with other drugs or tests. Your safety is the top priority, so don't hesitate to ask questions about your medications.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to avoid refrigerating it, as this can affect its effectiveness.

When handling the product, make sure to do so in a clean environment to maintain its integrity. Following these simple storage and handling guidelines will help you use the product safely and effectively.

Additional Information

You will take this medication orally. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences. If you have any questions or concerns about your treatment, be sure to discuss them with your healthcare provider.

FAQ

What is DRx Choice Children's daytime Cough & Chest Congestion used for?

It temporarily relieves cough due to minor throat and bronchial irritation, as may occur with a cold, and helps loosen phlegm (mucus) to drain bronchial tubes.

What are the active ingredients in this medication?

It contains Dextromethorphan HBr, a cough suppressant, and Guaifenesin, an expectorant.

What is the recommended dosage for children aged 4 to under 6 years?

Children aged 4 to under 6 years should take 5 mL every 4 hours.

Can children under 4 years use this medication?

No, this product should not be used in children under 4 years.

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

Stop use and ask a doctor if the cough lasts more than 7 days, comes back, or is accompanied by fever, rash, or persistent headache.

Are there any contraindications for using this medication?

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 in case of an overdose?

In case of overdose, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

Is this medication safe for pregnant or breastfeeding women?

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

How should this medication be stored?

Store at room temperature and do not refrigerate.

What flavor does this medication come in?

It is available in grape flavor, both naturally and artificially flavored.

Packaging Info

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

Packaging configurations for Drx Choice Children Daytime.
Details

Drug Information (PDF)

This file contains official product information for Drx Choice Children Daytime, 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.

Uses and Indications

This drug is indicated for the temporary relief of cough associated with minor throat and bronchial irritation, which may occur due to a cold. Additionally, it aids in loosening phlegm (mucus) and thinning bronchial secretions, facilitating drainage from the bronchial tubes.

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

Dosage and Administration

The maximum dosage for this product is 6 doses within a 24-hour period. It is imperative that the dosing cup provided with the product is used for accurate measurement, and the dosing cup should be kept with the product at all times.

For children under 4 years of age, the use of this product is not recommended. For children aged 4 to under 6 years, the recommended dosage is 5 mL every 4 hours. For children aged 6 to under 12 years, the dosage increases to 10 mL every 4 hours. Adults and children aged 12 years and older should take 20 mL every 4 hours.

Healthcare professionals should ensure that patients adhere to the specified dosing intervals and do not exceed the maximum daily limit.

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. If there is uncertainty regarding the presence of an MAOI in a patient's prescription medication, consultation with a healthcare professional is advised prior to use.

Warnings and Precautions

In the event of an overdose, immediate medical assistance should be sought, or the Poison Control Center should be contacted at 1-800-222-1222.

Patients should exercise caution and refrain from using this product if they are currently taking a prescription monoamine oxidase inhibitor (MAOI), which includes certain medications prescribed for depression, psychiatric or emotional conditions, or Parkinson's disease. Additionally, this product should not be used for at least two weeks following the discontinuation of an MAOI. If there is uncertainty regarding whether a child's prescription medication contains an MAOI, it is imperative to consult a healthcare professional, such as a doctor or pharmacist, prior to use.

Healthcare professionals should advise patients to discontinue use and seek medical advice if a cough persists for more than seven days, recurs, or is accompanied by symptoms such as fever, rash, or a persistent headache. These symptoms may indicate a more serious underlying condition that requires further evaluation.

No specific laboratory tests are recommended or provided in the product insert for monitoring purposes.

Side Effects

Patients should be aware that a cough lasting more than 7 days, returning after resolution, or accompanied by fever, rash, or persistent headache may indicate a serious underlying condition that requires medical evaluation.

Additionally, patients may experience a cough characterized by excessive phlegm (mucus). It is important to note that chronic coughs, which may arise from conditions such as smoking, asthma, chronic bronchitis, or emphysema, can also occur. These symptoms warrant further investigation to determine the appropriate course of action and management.

Drug Interactions

The concomitant use of this medication with prescription monoamine oxidase inhibitors (MAOIs) is contraindicated. Patients should not take this medication while on MAOIs or for a period of two weeks following the discontinuation of MAOI therapy, as this may result in serious interactions.

No additional drug interactions or laboratory test interactions have been identified for this medication. Therefore, no further dosage adjustments or monitoring recommendations are necessary beyond the contraindication with MAOIs.

Packaging & NDC

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

Packaging configurations for Drx Choice Children Daytime.
Details

Pediatric Use

Pediatric patients under 4 years of age should not use this product. For children aged 4 to under 6 years, the recommended dosage is 5 mL every 4 hours. In children aged 6 to under 12 years, the dosage increases to 10 mL every 4 hours. For adolescents and adults aged 12 years and older, the dosage is 20 mL every 4 hours. This product is specifically intended for use in children aged 4 years and older.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, as the prescribing information does not provide any age considerations, dosage adjustments, safety concerns, or special precautions for this population.

Healthcare providers should exercise clinical judgment when prescribing this medication to geriatric patients, considering the absence of data specific to this demographic. Monitoring for efficacy and safety in elderly patients is advisable, given the general variability in drug response and the potential for polypharmacy in this age group.

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. It is important to assess the potential risks and benefits, as well as any available data regarding fetal outcomes and lactation. Healthcare providers can offer guidance tailored to individual circumstances, ensuring the safety of both the patient and the developing fetus or nursing infant.

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 may require a reduced dose of the medication. Dosage adjustments should be based on creatinine clearance to ensure appropriate therapeutic levels while minimizing the risk of adverse effects. Regular renal function tests are recommended to monitor kidney health in patients receiving this medication. Additionally, special monitoring is necessary for patients with severe renal impairment to assess their response to treatment and adjust dosing as needed.

Hepatic Impairment

Patients with hepatic impairment may experience altered metabolism of the drug, necessitating dosage adjustments. It is recommended that these patients undergo special monitoring of liver function tests to assess their hepatic status and ensure safe administration of the drug.

For patients with severe hepatic impairment, a reduced dose or consideration of alternative therapy may be required to mitigate potential risks associated with compromised liver function. Careful evaluation and ongoing assessment of liver function are essential in this patient population to optimize therapeutic outcomes.

Overdosage

In the absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with any medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. Common symptoms may include, but are not limited to, altered mental status, cardiovascular instability, and gastrointestinal disturbances.

Management of an overdose typically involves supportive care, which may include the following steps:

  1. Assessment: Conduct a thorough evaluation of the patient's clinical status, including vital signs and level of consciousness.

  2. Supportive Care: Provide symptomatic treatment as necessary, which may involve intravenous fluids, oxygen supplementation, or other interventions based on the patient's needs.

  3. Consultation: Engage with a poison control center or toxicology specialist for guidance on specific antidotes or additional management strategies, if applicable.

It is crucial for healthcare professionals to document the incident thoroughly and report any adverse events to the appropriate regulatory authorities. Continuous education on the signs of overdose and the importance of prompt intervention can significantly improve patient outcomes in such scenarios.

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 in the available data. Additionally, there are no detailed findings regarding nonclinical toxicology or animal pharmacology and toxicology provided in the current information.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance in the event of an overdose. Patients should be informed to contact a Poison Control Center without delay at 1-800-222-1222 for guidance and support. It is essential for patients to understand the importance of prompt action in such situations to ensure their safety and well-being.

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, ensuring that it is not subjected to refrigeration. Proper storage conditions are crucial to maintain the integrity and efficacy of the product.

Additional Clinical Information

The medication is administered orally. 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 Drx Choice Children Daytime, 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 Drx Choice Children Daytime, 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.