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Warrior Pain Relief Roll-on

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Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2020
Label revision date
December 19, 2024
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2020
Label revision date
December 19, 2024
Manufacturer
Derma Care Research Labs, LLC
Registration number
M017
NDC root
72839-108

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 be looking for a solution to relieve pain, and this product is designed to help with that. It is suitable for adults and children aged 2 years and older, and you can apply it to the affected area up to 3 to 4 times daily.

This medication works by targeting pain directly where you need it, providing localized relief. If you have a child under 2 years of age, it's best to consult a doctor before use.

Uses

If you are looking for a treatment option, this medication can be applied to the affected area for adults and children aged 2 years and older. You should use it no more than 3 to 4 times a day. If your child is under 2 years old, it's important to consult a doctor before use.

This medication has not been reported to cause any teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects (which refers to other types of harmful effects that are not related to birth defects). Always follow the guidance provided by your healthcare professional for the best results.

Dosage and Administration

If you're looking for temporary relief from pain and itching, this medication can help. It's designed to provide quick comfort when you're experiencing these symptoms.

To use it effectively, follow the instructions provided by your healthcare provider or the product label. Make sure to apply or take the medication as directed, and remember that it's meant for short-term use. If your symptoms persist or worsen, be sure to consult with a healthcare professional for further advice.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. While there are no listed contraindications, controlled substance classifications, or concerns about abuse or dependence, you should take care to avoid accidental ingestion. If this occurs, seek professional assistance or contact a Poison Control Center immediately for guidance. Your safety is paramount, so please follow these instructions closely.

Side Effects

When using this product, it's important to follow the directions carefully. It is meant for external use only, so avoid contact with your eyes and do not apply it in large amounts, especially on raw or blistered skin. If your condition worsens, if symptoms last more than 7 days, or if they improve and then return within a few days, you should stop using the product and consult a doctor.

Warnings and Precautions

This product is for external use only, so be sure to follow the directions carefully. Avoid getting it in your eyes and do not apply it in large amounts, especially on raw or blistered skin. If your condition worsens, if symptoms last longer than 7 days, or if they improve and then come back within a few days, stop using the product and consult your doctor.

If you accidentally swallow this product, seek emergency medical help right away or contact a Poison Control Center for assistance. Your safety is important, so please take these precautions seriously.

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

It’s important to be cautious when considering any medication during pregnancy. For Warrior Pain Relief Roll-On Maximum Strength (lidocaine hcl 4% gel), there is no specific information available about its use during pregnancy, including safety concerns, dosage adjustments, or any special precautions.

If you are pregnant or planning to become pregnant, it’s best to consult with your healthcare provider before using this product to ensure it’s safe for you and your baby. Always prioritize open communication with your doctor about any medications you are considering.

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 known concerns about the product being passed into breast milk or any associated risks for your infant. This means you can use the product without worrying about its effects on your milk production or your baby's health.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 2 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 how this medication should be used by 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 a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions that may be present.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for personalized advice. They can monitor for any potential side effects and make recommendations based on individual health status.

Renal Impairment

If you have kidney problems, 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 instructions for the medication do not include special considerations for those with 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 kidney health. They can provide guidance tailored to your specific situation.

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).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and tests during your appointments.

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 not to freeze the product, as this can affect its effectiveness. Once you open the product, be sure to discard it after use to maintain safety and quality.

By following these simple storage and handling guidelines, you can help ensure that the product remains safe and effective for your needs.

Additional Information

You should apply this product to the affected area no more than 3 to 4 times daily if you are an adult or a child aged 2 years and older. If the user is under 2 years old, consult a doctor before use. Always follow the directions provided, avoid contact with your eyes, and do not apply large amounts, especially on raw or blistered skin.

If your condition worsens, symptoms last longer than 7 days, or if they improve and then return within a few days, stop using the product and consult a doctor. In case of accidental ingestion, seek professional help or contact a Poison Control Center immediately.

FAQ

How should I use this product?

For adults and children 2 years and older, apply to the affected area not more than 3 to 4 times daily. For children under 2 years of age, ask a doctor.

What should I do if I accidentally ingest this product?

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Are there any warnings I should be aware of?

This product is for external use only. Avoid contact with eyes and do not use in large quantities, especially over raw surfaces or blistered areas.

What should I do if my condition worsens?

Stop use and ask a doctor if the condition worsens, symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days.

Is this product safe to use during pregnancy or while nursing?

There is no specific information regarding use during pregnancy or lactation in the product insert.

How should I store this product?

Store at room temperature, protect from light, and do not freeze. Discard after opening.

Are there any contraindications or drug interactions?

No contraindications or drug interactions were mentioned in the provided text.

Packaging Info

Below are the non-prescription pack sizes of Warrior Pain Relief Roll-on (lidocaine hcl 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Warrior Pain Relief Roll-on.
Details

Drug Information (PDF)

This file contains official product information for Warrior Pain Relief Roll-on, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product, identified by SPL code 34089-3, is a topical analgesic formulated to provide temporary relief from minor aches and pains. It contains menthol as the active ingredient and is packaged in a 3 oz (85 g) container. The formulation features a roll-on applicator, facilitating ease of application. Inactive ingredients include water, alcohol, glycerin, carbomer, triethanolamine, fragrance, and colorant.

Uses and Indications

This drug is indicated for the topical treatment of affected areas in adults and children aged 2 years and older. It should be applied no more than 3 to 4 times daily. For children under 2 years of age, consultation with a healthcare professional is advised prior to use.

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

Dosage and Administration

For the temporary relief of pain and itching, the recommended dosage should be determined based on the specific needs of the patient. Healthcare professionals are advised to assess the severity of symptoms and individual patient response when prescribing.

The administration route and method will depend on the formulation of the medication. It is essential to follow the manufacturer's guidelines for preparation and administration techniques to ensure optimal efficacy and safety.

Dosing intervals should be established according to the patient's condition and response to treatment. Regular monitoring is recommended to adjust the dosage as necessary, ensuring that the patient receives the most effective relief while minimizing potential side effects.

Contraindications

There are no specific contraindications listed for this product. However, in the event of accidental ingestion, it is imperative to seek professional assistance or contact a Poison Control Center immediately.

Warnings and Precautions

The product is intended for external use only. Healthcare professionals should advise patients to adhere strictly to the directions for use, ensuring that the product does not come into contact with the eyes. It is imperative to avoid applying the product in large quantities, particularly on raw surfaces or blistered areas, to prevent potential adverse effects.

Patients should be instructed to discontinue use and consult a healthcare provider if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. This precaution is essential to ensure that any underlying conditions are appropriately evaluated and managed.

In the event of accidental ingestion, immediate medical assistance should be sought. Patients or caregivers are advised to contact a Poison Control Center without delay to receive appropriate guidance and intervention.

Overall, careful monitoring of the patient's condition is recommended, and healthcare professionals should remain vigilant for any signs of worsening symptoms or adverse reactions during the course of treatment.

Side Effects

Patients should be aware that this product is for external use only. It is imperative to use the product strictly as directed, avoiding contact with the eyes. Additionally, patients should refrain from using the product in large quantities, especially over raw surfaces or blistered areas.

In the event that the condition worsens, or if symptoms persist for more than 7 days, patients are advised to discontinue use and consult a healthcare professional. Furthermore, if symptoms clear up and then recur within a few days, it is also recommended to seek medical advice.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Warrior Pain Relief Roll-on (lidocaine hcl 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Warrior Pain Relief Roll-on.
Details

Pediatric Use

Pediatric patients aged 2 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 before use.

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

There is no information available regarding the use of Warrior Pain Relief Roll-On Maximum Strength (lidocaine hcl 4% gel) during pregnancy. As such, the safety of this product in pregnant patients has not been established, and there are no known dosage modifications or special precautions recommended for use in this population. Healthcare professionals should consider the lack of data when advising women of childbearing potential and weigh the potential risks and benefits before recommending this product during pregnancy.

Lactation

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

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 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 initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of antidotes or specific treatments should be considered based on the substance involved and the clinical presentation. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

Documentation of the incident, including the substance, amount ingested, and time of ingestion, is crucial for effective management and treatment planning.

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

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to seek professional assistance or contact a Poison Control Center immediately in the event of accidental ingestion. It is important for patients to understand the potential risks associated with unintentional consumption and to act swiftly to ensure their safety.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Additionally, once opened, the product must be discarded to ensure safety and efficacy.

Additional Clinical Information

Patients aged 2 years and older are advised to apply the product to the affected area no more than 3 to 4 times daily. For children under 2 years of age, consultation with a doctor is recommended prior to use.

Clinicians should counsel patients to use the product only as directed, avoiding contact with the eyes and refraining from applying it in large quantities, especially on raw surfaces or blistered areas. Patients should discontinue use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. In the event of accidental ingestion, patients should seek professional assistance or contact a Poison Control Center immediately.

Drug Information (PDF)

This file contains official product information for Warrior Pain Relief Roll-on, 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 Warrior Pain Relief Roll-on, 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

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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.