Symptom checker
Select audience type

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

ADD CONDITION

items per page

Will Relieve Roll-on

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 3.2 g/88 mL
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2022
Label revision date
July 13, 2023
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 3.2 g/88 mL
Other brand names
Dosage form
Gel
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 2022
Label revision date
July 13, 2023
Manufacturer
Will Perform, PBC
Registration number
part348
NDC root
82630-002
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

WILL™ is a fast-acting pain relief roll-on that contains lidocaine, a medication that helps numb the area where it is applied. This product is designed to provide temporary relief from pain, making it a convenient option for those seeking quick comfort from discomfort.

With a volume of 3 fluid ounces (88 mL), WILL™ is easy to use and features branding by the well-known athlete Serena Williams, adding a touch of recognition to your pain relief routine. Whether you're dealing with muscle aches or other types of pain, this roll-on aims to help you feel better swiftly.

Uses

You can use this medication for the temporary relief of pain. It is designed to help alleviate discomfort, making it easier for you to go about your daily activities.

Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this medication. Additionally, there are no nonteratogenic effects (which refer to other types of harmful effects that do not involve birth defects) reported. This makes it a safer option for managing your pain.

Dosage and Administration

When using this medication, you should apply a thin layer directly to the affected area of your skin. For adults and children over 12 years old, this should be done every 6 to 8 hours, but make sure not to apply it more than three times in a 24-hour period.

If you are considering using this medication for a child who is 12 years old or younger, it’s important to consult with a doctor first to ensure it’s safe and appropriate for them. Always follow these guidelines to help ensure effective and safe use of the medication.

What to Avoid

It's important to use this product safely to avoid potential complications. You should not apply it to large areas of your body, on cuts, irritated, or swollen skin, or on puncture wounds. Additionally, avoid using it for more than one week without consulting your doctor.

While using this product, make sure to keep it away from your eyes and mucous membranes. Do not cover the area with a bandage or apply local heat, such as heating pads, and avoid using it alongside other topical pain relievers. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

When using this product, it's important to be aware of potential side effects. You should stop using it and consult a doctor if your condition worsens, if you notice redness or irritation, or if symptoms persist for more than seven days or return shortly after improvement.

This product is for external use only and should not be applied to large areas of the body, cuts, irritated skin, or puncture wounds. Avoid contact with your eyes and mucous membranes, and do not use it alongside other topical pain relievers. If you are pregnant or breastfeeding, please consult a healthcare professional before use. Always keep it out of reach of children and pets, and seek immediate medical help if swallowed.

Warnings and Precautions

This product is for external use only and is flammable, so be sure to keep it away from heat and open flames. Avoid using it on large areas of your body, on cuts, irritated skin, or puncture wounds. It’s important to follow the instructions on the packaging carefully and not to use it for more than one week without consulting your doctor. Make sure to keep it away from your eyes and mucous membranes, and do not apply heat or bandage the area where you use it. Additionally, do not use it alongside other topical pain relievers.

If you accidentally swallow this product, seek medical help or contact a Poison Control Center immediately. You should also stop using it and call your doctor if your condition worsens, if you notice any redness or irritation, or if your symptoms last longer than seven days or return shortly after improvement.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and get checked by a medical professional.

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 professional 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 benefits for both you and your baby. Your healthcare provider can help you make informed decisions about your health and the health of your nursing infant.

Pediatric Use

Before using this medication for children aged 12 years or younger, it’s important to consult with a doctor. For those over 12 years old, you can apply a thin layer of the medication to the affected area every 6 to 8 hours, but be sure not to exceed three applications in a 24-hour period.

Always keep the medication out of reach of children and pets. If the medication is swallowed, seek medical help or contact a Poison Control Center immediately.

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 prioritize open communication with your healthcare team, especially regarding any changes in health or concerns about side effects. Your safety and well-being are paramount, so don’t hesitate to ask questions or seek guidance tailored to your unique situation.

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 may affect you if your kidneys are not functioning properly.

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 help monitor your condition and make any necessary adjustments to your treatment plan.

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 and appropriate for your liver health. They can help you understand how to manage your treatment effectively.

Drug Interactions

It's important to be cautious when using certain medications together. Specifically, you should avoid using this medication at the same time as other topical analgesics (pain-relieving creams or gels applied to the skin). Mixing these products can increase the risk of side effects or reduce their effectiveness.

Always discuss any medications you are taking, including over-the-counter products, with your healthcare provider. They can help ensure that your treatment is safe and effective, and they can provide guidance on how to use your medications properly.

Storage and Handling

To ensure the best performance and safety of your product, store it at room temperature, away from excessive heat or open flames. It's important to keep the product protected from light to maintain its effectiveness. Once you open the product, please remember to discard it after use to avoid any potential safety issues. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply a thin layer of the medication to the affected area every 6 to 8 hours, but do not exceed three applications in a 24-hour period if you are an adult or a child over 12 years old. If the patient is 12 years old or younger, consult a doctor before use.

If you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this medication. Always keep it out of reach of children and pets, and if swallowed, seek medical help or contact a Poison Control Center immediately.

FAQ

What is WILL™?

WILL™ is a fast-acting pain relief roll-on that contains lidocaine and comes in a volume of 3 FL OZ (88 mL).

What is the primary use of WILL™?

WILL™ is indicated for the temporary relief of pain.

How should adults and children over 12 years use WILL™?

Apply a thin layer over the affected area every 6 to 8 hours, not exceeding 3 applications in a 24-hour period.

What should children 12 years or younger do before using WILL™?

Children 12 years or younger should ask a doctor before use.

Are there any teratogenic effects associated with WILL™?

No teratogenic effects are mentioned for WILL™.

What precautions should I take when using WILL™?

Do not use on large areas of the body, on cuts, irritated or swollen skin, or puncture wounds. Avoid contact with eyes and mucous membranes.

What should I do if I experience irritation or worsening conditions while using WILL™?

Stop using WILL™ and consult a doctor if conditions worsen, redness is present, or irritation develops.

What should I do if I swallow WILL™?

If swallowed, get medical help or contact a Poison Control Center immediately.

Can I use WILL™ with other topical analgesics?

No, do not use WILL™ at the same time as other topical analgesics.

What storage conditions are recommended for WILL™?

Store WILL™ at room temperature, away from excessive heat or open flame, and protect it from light.

Packaging Info

Below are the non-prescription pack sizes of Will Relieve Roll-on (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Will Relieve Roll-on.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

WILL™ PERFORM, developed by Serena Williams, is a fast-acting roll-on formulation designed for pain relief. The active ingredient in this product is lidocaine, which is known for its local anesthetic properties. The product is available in a dosage form of 3 fluid ounces (88 mL).

Uses and Indications

This drug is indicated for the temporary relief of pain.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

For adults and children over 12 years of age, a thin layer of the medication should be applied to the affected area every 6 to 8 hours. It is important not to exceed three applications within a 24-hour period to avoid potential adverse effects.

For children aged 12 years or younger, it is recommended to consult a physician prior to use to ensure safety and appropriateness of treatment.

Contraindications

Use of this product is contraindicated in the following situations:

Application on large areas of the body, or on cut, irritated, or swollen skin is prohibited due to the potential for increased systemic absorption and adverse effects. The product should not be applied to puncture wounds, as this may lead to complications or infection.

Prolonged use beyond one week without consulting a healthcare professional is contraindicated to prevent potential misuse or exacerbation of underlying conditions.

During use, contact with eyes and mucous membranes must be avoided to prevent irritation or injury. Additionally, the application of bandages, local heat (such as heating pads), or medicated patches to the area of use is not recommended, as these practices may enhance absorption and increase the risk of adverse reactions. Concurrent use with other topical analgesics is also contraindicated to avoid potential additive effects and toxicity.

Warnings and Precautions

For external use only. This product is flammable; therefore, it must be kept away from excessive heat or open flame.

General precautions should be observed to ensure safe use. The product should not be applied to large areas of the body or on cut, irritated, or swollen skin. It is contraindicated for use on puncture wounds. Users are advised not to exceed one week of use without consulting a healthcare professional. It is imperative to use the product only as directed, adhering to all instructions and warnings provided on the carton. Contact with eyes and mucous membranes must be avoided. Additionally, the area of application should not be bandaged, nor should local heat (such as heating pads) or medicated patches be applied concurrently. The use of other topical analgesics at the same time is also contraindicated.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Patients should discontinue use and consult a healthcare provider if any of the following occur: worsening of conditions, presence of redness, development of irritation, or if symptoms persist beyond seven days or resolve only to recur within a few days.

Side Effects

Patients should be aware that this product is intended for external use only. It is contraindicated for application on large areas of the body, on cut, irritated, or swollen skin, and on puncture wounds. The product should not be used for more than one week without consulting a healthcare professional.

When using this product, it is essential to adhere strictly to the directions provided. Patients should avoid contact with the eyes and mucous membranes, and should not bandage or apply local heat, such as heating pads or medicated patches, to the area of use. Concurrent use with other topical analgesics is also not recommended.

Patients are advised to discontinue use and consult a doctor if any of the following occur: worsening of conditions, presence of redness, development of irritation, or if symptoms persist for more than seven days or resolve and then recur within a few days.

Additional considerations include the need for pregnant or breastfeeding individuals to seek advice from a healthcare professional prior to use. The product should be kept out of reach of children and pets; in the event of ingestion, immediate medical assistance or contact with a Poison Control Center is necessary.

Drug Interactions

Concurrent use of this medication with other topical analgesics is contraindicated. The combination may increase the risk of adverse effects without providing additional therapeutic benefit. It is advised to avoid using multiple topical analgesics simultaneously to ensure patient safety and efficacy of treatment. Monitoring for any signs of irritation or adverse reactions is recommended if there is a need to switch to or from another topical analgesic.

Packaging & NDC

Below are the non-prescription pack sizes of Will Relieve Roll-on (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Will Relieve Roll-on.
Details

Pediatric Use

Pediatric patients 12 years of age or younger should consult a healthcare professional before use. For adolescents and adults over 12 years, the recommended application is a thin layer over the affected area every 6 to 8 hours, with a maximum of 3 applications within a 24-hour period.

It is essential to keep the product out of reach of children and pets. In the event of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

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 considered, as the effects on fetal outcomes and breastfeeding infants are not fully established. It is essential for women of childbearing potential to discuss their individual circumstances with their healthcare provider to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a healthcare professional prior to using this medication. There is currently no available data regarding the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when considering the use of this medication during lactation.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of guidance necessitates careful clinical judgment.

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 overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous monitoring and evaluation are advised to ensure patient safety and effective resolution of any complications arising from the overdosage.

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 understanding of the potential toxicological profile in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children and pets to prevent accidental ingestion. Instruct patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately.

It is essential for patients to use the medication only as directed. They should be encouraged to read and follow all directions and warnings provided on the carton to ensure safe and effective use.

Healthcare providers should also inform patients to avoid contact with eyes and mucous membranes, as this may lead to irritation or adverse effects. Additionally, patients should be cautioned against bandaging or applying local heat, such as heating pads, or using a medicated patch on the area of application, as these actions may exacerbate side effects or reduce efficacy.

Finally, it is important to advise patients not to use this medication concurrently with other topical analgesics, as this may increase the risk of adverse reactions.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which should be referenced for accurate identification. It is essential to store the product at room temperature, ensuring that it is kept away from excessive heat and open flame to maintain its integrity. Additionally, the product must be protected from light exposure to prevent degradation. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application of a thin layer over the affected area every 6 to 8 hours for adults and children over 12 years, not exceeding three applications within a 24-hour period. For children aged 12 years or younger, it is advised to consult a doctor prior to use.

Clinicians should counsel patients to seek advice from a healthcare professional if they are pregnant or breastfeeding. Additionally, it is important to keep the product out of reach of children and pets. In the event of accidental ingestion, patients should seek medical assistance or contact a Poison Control Center immediately.

Drug Information (PDF)

This file contains official product information for Will Relieve 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 Will Relieve 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

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.