Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Chloraseptic Warming Green Tea

Last content change checked dailysee data sync status

Active ingredient
Benzocaine 15 mg
Other brand names
Dosage form
Lozenge
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2012
Label revision date
March 6, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 15 mg
Other brand names
Dosage form
Lozenge
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 2012
Label revision date
March 6, 2026
Manufacturer
Prestige Brands Holdings, Inc.
NDC root
67172-020
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

Chloraseptic is a type of oral anesthetic that comes in the form of lozenges. It contains benzocaine, which helps to temporarily relieve minor irritation, pain, and discomfort in the throat and mouth. These lozenges are designed to soothe sore throats and sore mouths, making them a helpful option when you're experiencing these common issues.

In addition to benzocaine, Chloraseptic lozenges are enriched with warming ingredients and green tea, along with real honey, which can provide a comforting effect. Each package contains 18 lozenges, making it easy to have on hand when you need relief from throat discomfort.

Uses

You can use this medication to temporarily relieve occasional minor irritation, pain, sore throat, and sore mouth. It’s designed to help ease discomfort when you’re feeling under the weather.

Rest assured, there are no teratogenic effects (which means it doesn’t cause birth defects) associated with this medication, making it a safer option for those who may be concerned about such risks.

Dosage and Administration

If you are an adult or a child aged 6 years and older, you can take 1 lozenge every 2 hours as needed. It's important to let the lozenge dissolve slowly in your mouth for the best effect.

However, if you are caring for a child under 6 years of age, this medication is not recommended for them. Always follow these guidelines to ensure safe and effective use of the lozenges.

What to Avoid

It's important to follow the recommended dosage when using this medication. Exceeding the recommended amount can lead to unwanted effects. Always use the medication as directed to ensure your safety and well-being. If you have any questions or concerns about your dosage, please consult your healthcare provider for guidance.

Side Effects

If you have a history of allergies to local anesthetics like procaine, butacaine, or benzocaine, it's important not to use this product. Be aware that if you experience a severe or persistent sore throat, especially if it's accompanied by high fever, headache, nausea, or vomiting, you should consult a doctor right away. Additionally, do not use this product for more than two days or give it to children under six years old.

You should stop using this product and contact a dentist or doctor if your sore mouth symptoms do not improve within seven days, or if you notice any irritation, pain, or redness that persists or worsens. Also, seek medical advice if you develop swelling, a rash, or a fever.

Warnings and Precautions

You should avoid using this product if you have a history of allergies to local anesthetics, such as procaine, butacaine, benzocaine, or any other “caine” anesthetics. If you experience a severe or persistent sore throat, especially if it comes with a high fever, headache, nausea, or vomiting, it’s important to consult a doctor right away. Additionally, do not use this product for more than 2 days or give it to children under 6 years of age.

If your sore mouth symptoms do not improve within 7 days, or if you notice any irritation, pain, or redness that persists or worsens, you should stop using the product and contact your dentist or doctor. Be alert for any swelling, rash, or fever, as these may require medical attention. In the event of an overdose or accidental poisoning, seek medical help immediately or contact a Poison Control Center.

Overdose

If you suspect an overdose or accidental poisoning, it’s crucial to seek medical help immediately or contact a Poison Control Center. Signs of an overdose can vary, but they may include unusual symptoms that require prompt attention.

Always err on the side of caution—if you’re unsure whether the symptoms you or someone else is experiencing are related to an overdose, don’t hesitate to reach out for professional assistance. Your health and safety are the top priority.

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

It's important to be cautious when considering this product for your child. You should not use it for children under 6 years of age, as it is contraindicated (not recommended) for this age group.

For children aged 6 years and older, the recommended dosage is one lozenge every two hours as needed. Always ensure you follow these guidelines to keep your child safe and healthy.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so discussing any concerns with a doctor is essential for ensuring safety and effectiveness.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment is safe and effective for your specific condition. They can help determine the best approach for managing your health, especially if you have concerns about your kidneys.

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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe for your liver health. They can help determine the best approach for your treatment based on your individual circumstances.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at temperatures below 25°C (77°F). It's important to keep it away from moisture, as this can affect its effectiveness and safety.

When handling the product, make sure to do so in a clean environment to maintain its integrity. Always follow any additional safety guidelines provided with the product to ensure safe usage and disposal.

Additional Information

No further information is available.

FAQ

What is Chloraseptic?

Chloraseptic is a benzocaine oral anesthetic and analgesic lozenge that temporarily relieves occasional minor irritation, pain, sore throat, and sore mouth.

Who can use Chloraseptic?

Chloraseptic is intended for adults and children 6 years of age and over. It is contraindicated for children under 6 years of age.

How should I take Chloraseptic?

You should take 1 lozenge every 2 hours as needed, allowing it to dissolve slowly in your mouth.

Are there any warnings associated with Chloraseptic?

Yes, do not use Chloraseptic if you have a history of allergy to local anesthetics. Consult a doctor if you have a severe or persistent sore throat.

What should I do if my symptoms do not improve?

If sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persists or worsens, you should stop use and consult a dentist or doctor.

Is Chloraseptic safe to use during pregnancy or breastfeeding?

If you are pregnant or breastfeeding, you should ask a health professional before using Chloraseptic.

What should I do in case of overdose?

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

How should I store Chloraseptic?

Store Chloraseptic below 25°C and protect it from moisture.

Packaging Info

Below are the non-prescription pack sizes of Chloraseptic Warming Green Tea (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Chloraseptic Warming Green Tea.
Details

Drug Information (PDF)

This file contains official product information for Chloraseptic Warming Green Tea, 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 drug.

Uses and Indications

This drug is indicated for the temporary relief of occasional minor irritation, pain, sore throat, and sore mouth.

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

Dosage and Administration

Adults and children aged 6 years and older are instructed to take 1 lozenge every 2 hours as needed. The lozenge should be allowed to dissolve slowly in the mouth to ensure optimal absorption and effectiveness.

The use of this medication is contraindicated in children under 6 years of age.

Contraindications

There are no contraindications listed for this product. However, it is essential to adhere to the recommended dosage guidelines to avoid potential adverse effects. Exceeding the recommended dosage may lead to complications.

Warnings and Precautions

Patients with a known history of allergy to local anesthetics, including procaine, butacaine, benzocaine, or other “caine” anesthetics, should not use this product due to the risk of severe allergic reactions.

Severe or persistent sore throat, particularly when accompanied by high fever, headache, nausea, or vomiting, may indicate a serious condition. In such cases, it is imperative to consult a healthcare professional promptly. The product should not be used for more than two days, and it is contraindicated in children under six years of age.

Healthcare professionals should advise patients to discontinue use and seek guidance from a dentist or physician if any of the following occur: sore mouth symptoms do not improve within seven days; irritation, pain, or redness persists or worsens; or if swelling, rash, or fever develops.

In the event of an overdose or accidental poisoning, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

Patients should be aware of the potential adverse reactions associated with this product. Serious adverse reactions may include severe or persistent sore throat, particularly when accompanied by high fever, headache, nausea, and vomiting. Such symptoms may indicate a serious condition, and patients are advised to consult a healthcare professional promptly.

Additionally, patients with a known history of allergy to local anesthetics, including procaine, butacaine, benzocaine, or other “caine” anesthetics, should refrain from using this product due to the risk of allergic reactions.

Common adverse reactions may necessitate discontinuation of use and consultation with a dentist or doctor. These include sore mouth symptoms that do not improve within 7 days, as well as any irritation, pain, or redness that persists or worsens. Patients should also seek medical advice if they experience swelling, rash, or fever during treatment.

It is important to note that this product should not be used for more than 2 days and is not recommended for children under 6 years of age.

Drug Interactions

There are currently no documented drug interactions associated with the use of this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Chloraseptic Warming Green Tea (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Chloraseptic Warming Green Tea.
Details

Pediatric Use

Pediatric patients under 6 years of age should not use this product due to safety concerns. For pediatric patients aged 6 years and older, the recommended dosage is 1 lozenge every 2 hours as needed. Care should be taken to adhere to this dosing schedule to ensure safety and efficacy in this age group.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any adverse effects or changes in therapeutic response, given the lack of targeted data for 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 prescribing information regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the absence of detailed guidance 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 the use of this medication. Consequently, there are no 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 or accidental poisoning, it is imperative to seek immediate medical assistance or contact a Poison Control Center. Prompt action is crucial to mitigate potential adverse effects associated with overdosage.

Healthcare professionals should be aware that symptoms of overdose may vary depending on the substance involved. Therefore, a thorough assessment of the patient's condition is essential.

Management of an overdose typically involves supportive care and symptomatic treatment. The specific interventions may depend on the nature of the overdose and the patient's clinical presentation. Continuous monitoring of vital signs and supportive measures should be implemented as necessary.

In all cases of suspected overdose, timely communication with poison control and adherence to established protocols for overdose management are recommended to ensure optimal patient outcomes.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the use of the compound in these contexts.

Postmarketing Experience

Postmarketing experience has revealed reports of allergic reactions, including anaphylaxis, in patients using benzocaine products. Additionally, cases of methemoglobinemia have been reported, particularly in infants and young children. Other adverse reactions noted include skin reactions such as rash and urticaria.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. In the event of an overdose or accidental poisoning, patients should seek medical assistance or contact a Poison Control Center immediately.

Patients should be informed to discontinue use and consult a dentist or doctor if symptoms of a sore mouth do not improve within 7 days. Additionally, they should be instructed to stop using the product and seek medical advice if they experience persistent or worsening irritation, pain, or redness. Patients should also be made aware that they need to stop use and consult a healthcare professional if they develop swelling, rash, or fever.

It is important to remind patients not to exceed the recommended dosage while using this product to ensure their safety and well-being.

Storage and Handling

The product is supplied in configurations that include specific NDC numbers. It should be stored at temperatures below 25°C to maintain its efficacy. Additionally, it is essential to protect the product from moisture to ensure its integrity and stability. Proper handling and storage conditions are critical for preserving the quality of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Chloraseptic Warming Green Tea, 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 Chloraseptic Warming Green Tea, 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.

Learn more in our Editorial Policy

Last AI update:

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.