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Chiggerex 2x Medicated

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This product has been discontinued

Active ingredient
Benzocaine 10 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2013
Label revision date
October 4, 2017
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 10 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
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 2013
Label revision date
October 4, 2017
Manufacturer
Product Quest Mfg
Registration number
part348
NDC root
64048-1111
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

You may find relief from pain and itching caused by insect bites, such as those from chiggers, red bugs, ticks, and mosquitoes, with this medication. It is designed to temporarily alleviate discomfort associated with these bites, helping you feel more comfortable.

Uses

If you're dealing with discomfort from insect bites, this medication can help. It temporarily relieves pain and itching caused by bites from chiggers, red bugs, ticks, and mosquitoes. This means you can find some relief from the annoying sensations that come with these pesky bites, allowing you to feel more comfortable.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can apply the medication directly to the affected area of your skin. Make sure to do this no more than 3 to 4 times a day for the best results.

For children under 2 years of age, it’s important to consult a doctor before using this medication. This ensures that it’s safe and appropriate for their specific needs. Always follow these guidelines to help manage your condition effectively.

What to Avoid

There are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. Additionally, there are no explicit instructions indicating that you should not take or use this medication. Always consult with your healthcare provider for personalized advice and to ensure this medication is appropriate for you.

Side Effects

When using this product, it's important to remember that it is for external use only and should not come into contact with your eyes. If you notice a rash, if your condition worsens, or if symptoms persist for more than 7 days or return shortly after improvement, you should stop using the product and consult a doctor.

Additionally, keep this product out of reach of children. If it is swallowed, please contact a Poison Control Center right away for assistance.

Warnings and Precautions

This product is for external use only, so please avoid getting it in your eyes. It's important to keep it out of reach of children. If a child accidentally swallows it, contact a Poison Control Center right away.

You should stop using this product and consult your doctor if you notice a rash, if your condition worsens, or if your symptoms last more than 7 days or improve only to return within a few days. Taking these precautions will help ensure your safety while using the product.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, it’s important to act quickly. Contact a Poison Control Center immediately for guidance. They can provide you with the necessary steps to take based on the specific situation.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, seek immediate medical help. Remember, acting quickly can make a significant difference in ensuring safety and health.

Pregnancy Use

When it comes to using CHIGGEREX 2X MEDICATED (benzocaine 10.0% ointment) during pregnancy, there is currently no information available about its safety, recommended dosage, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product. They can help you understand any potential risks and guide you on the best options for your situation. Always prioritize your health and the health of your baby by seeking professional advice.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there are no statements indicating that this product is excreted in breast milk or that it poses any risk to your infant. This means you can use it without concern for affecting your milk production or your baby's health. Always consult with your healthcare provider if you have any questions or concerns about medications while breastfeeding.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 12 years and older, you can apply it to the affected area up to 3 to 4 times a day. However, if your child is under 2 years old, you should consult a doctor before use to ensure safety and proper care. Always prioritize your child's health by following these recommendations closely.

Geriatric Use

While there is no specific information about the use of CHIGGEREX 2X MEDICATED (benzocaine 10.0% ointment) in older adults, it’s important to approach any new medication with caution. Since the drug insert does not mention dosage adjustments or safety concerns for elderly patients, you should consult with a healthcare professional before using this ointment. They can provide personalized advice based on your health status and any other medications you may be taking. Always prioritize safety and ensure that any treatment is appropriate for your individual needs.

Renal Impairment

If you have kidney issues, it's important to know that there are no specific guidelines, dosage adjustments, or monitoring recommendations provided for your condition in the available information. This means that the standard information does not address how your kidney health might affect the use of this medication.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can provide guidance tailored to your kidney health and any necessary precautions.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

Drug Interactions

It's great to know that there are no reported interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective, and helps avoid any potential issues.

Always keep your healthcare provider informed about any changes in your health or medications, as they can provide personalized advice tailored to your specific situation. Your safety and well-being are the top priority!

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important to keep the tube tightly closed when not in use to maintain its integrity. Once you open the tube, please remember to discard it after use to ensure safety and effectiveness. Following these simple guidelines will help you handle the product safely and effectively.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged 12 years and older. If the patient is under 2 years old, it's important to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or postmarketing experiences related to this medication.

FAQ

What is the purpose of this drug?

This drug temporarily relieves pain and itching due to chigger bites, red bug bites, ticks, and mosquito bites.

How should I use this drug?

Adults and children 12 years of age and older should apply it to the affected area no more than 3 to 4 times daily. Children under 2 years of age should consult a doctor.

Are there any warnings I should be aware of?

Yes, this product is for external use only. Avoid contact with the eyes, and stop use if a rash occurs, the condition worsens, or symptoms last more than 7 days.

What should I do if I swallow this product?

Keep it out of reach of children, and if swallowed, contact a Poison Control Center immediately.

Is there any information regarding use during pregnancy or nursing?

There is no specific information provided regarding the use of this product during pregnancy or nursing.

How should I store this drug?

Store at room temperature, protect from light, and keep the tube tightly closed when not in use. Discard after opening.

Packaging Info

Below are the non-prescription pack sizes of Chiggerex 2x Medicated (benzocaine 10.0%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Chiggerex 2x Medicated.
Details

Drug Information (PDF)

This file contains official product information for Chiggerex 2x Medicated, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with chigger bites, red bug bites, tick bites, and mosquito bites. It is intended for use in patients experiencing discomfort from these specific insect bites.

Limitations of Use: This product is not intended for long-term use and should be applied only as directed for symptomatic relief.

Dosage and Administration

For adults and children aged 12 years and older, the recommended application is to the affected area, not exceeding 3 to 4 times daily.

For children under 2 years of age, it is advised to consult a healthcare professional prior to use.

Contraindications

There are no contraindications listed for this product. It is important to evaluate individual patient circumstances and consult relevant clinical guidelines when considering its use.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes while using this product. In the event of a rash, worsening of the condition, or if symptoms persist for more than 7 days or resolve and then recur within a few days, the user should discontinue use and consult a healthcare professional.

This product must be kept out of reach of children. In the case of accidental ingestion, immediate contact with a Poison Control Center is advised.

No specific general precautions or laboratory tests are required for the safe use of this product.

Side Effects

Patients using this product should be aware that it is intended for external use only and must avoid contact with the eyes. In the event of a rash, worsening of the condition, or if symptoms persist for more than 7 days or resolve and then recur within a few days, patients are advised to discontinue use and consult a healthcare professional.

Additionally, it is crucial to keep this product out of reach of children. If ingested, immediate contact with a Poison Control Center is recommended.

Drug Interactions

There are no documented drug interactions associated with the use of this medication. Additionally, there are no reported interactions between this drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Chiggerex 2x Medicated (benzocaine 10.0%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Chiggerex 2x Medicated.
Details

Pediatric Use

Pediatric patients aged 12 years and older may apply the medication to the affected area up to 3 to 4 times daily. For children under 2 years of age, it is advised to consult a doctor prior to use.

Geriatric Use

There is no specific information regarding the use of CHIGGEREX 2X MEDICATED (benzocaine 10.0% ointment) in geriatric patients. The prescribing information does not provide guidance on dosage adjustments, safety concerns, or special precautions for elderly patients. Therefore, healthcare providers should exercise caution when considering the use of this medication in the geriatric population, as individual patient factors may necessitate careful monitoring and assessment.

Pregnancy

There is currently no information available regarding the use of CHIGGEREX 2X MEDICATED (benzocaine 10.0% ointment) during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Healthcare professionals should exercise caution when considering the use of this medication in women of childbearing potential, as the lack of data precludes a comprehensive assessment of potential risks to fetal outcomes. It is advisable to weigh the benefits against any unknown risks when prescribing this medication to pregnant patients.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there are no statements concerning the potential for excretion in breast milk or any associated risks to breastfed infants during lactation.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of 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 available information.

Overdosage

In the event of an overdosage, immediate action is crucial. If the substance is ingested, it is imperative to contact a Poison Control Center without delay.

Healthcare professionals should be aware that symptoms of overdosage may vary depending on the specific substance involved. Monitoring for any adverse effects is essential, and appropriate management should be initiated based on the clinical presentation and guidance from the Poison Control Center.

In cases of suspected overdosage, supportive care may be necessary, and further medical evaluation should be conducted to determine the extent of the overdose and to implement any required interventions.

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 question. Further studies may be necessary to fully evaluate the nonclinical toxicology profile.

Postmarketing Experience

No postmarketing experience details are available for SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important for patients to understand the potential risks associated with improper access to the medication by young children. Providers should emphasize the necessity of storing the medication in a secure location, away from areas where children may have access.

Storage and Handling

The product is supplied in a tube format, with specific handling and storage requirements to ensure its integrity and efficacy. It should be stored at room temperature, away from direct light exposure. To maintain the quality of the product, it is essential to keep the tube tightly closed when not in use. Additionally, the product should be discarded after opening to prevent any potential degradation or contamination.

Additional Clinical Information

The medication is administered topically, with the recommended frequency for adults and children aged 12 years and older being 3 to 4 applications to the affected area daily. For children under 2 years of age, it is advised to consult a doctor prior to use. No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Chiggerex 2x Medicated, 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 Chiggerex 2x Medicated, 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.