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Rugby Lidocaine

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Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2018
Label revision date
November 24, 2025
Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2018
Label revision date
November 24, 2025
Manufacturer
Rugby Laboratories
Registration number
M017
NDC root
0536-1139

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

RUGBY is a pain-relieving cream designed to temporarily relieve minor pain. It contains a maximum strength of 4% lidocaine, which is a local anesthetic that works by numbing the area where it is applied. This makes it useful for soothing discomfort from various minor aches and pains.

The cream comes in a 15g (0.52 oz) tube, making it easy to apply directly to the affected area for quick relief. Whether you're dealing with muscle soreness, joint pain, or other minor discomforts, RUGBY can help provide the soothing effect you need.

Uses

You can use this medication to temporarily relieve minor pain. It’s designed to help you feel more comfortable when dealing with everyday aches and discomforts. Rest assured, there are no known 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

When using this medication, if you are an adult or a child over 12 years old, you should apply a thin layer to the affected area every 6 to 8 hours. However, make sure not to exceed more than 3 applications in a 24-hour period. This helps ensure that you are using the medication safely and effectively.

If you have a child under 12 years old, it’s important to consult a doctor before using this medication. They can provide guidance on the appropriate treatment for younger children. Always follow these instructions carefully to achieve the best results.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should not apply it to large areas of your body or on any cut, irritated, or swollen skin. Additionally, avoid using it on puncture wounds. If you find that you need to use it for more than one week, please consult your doctor first.

Make sure to keep it away from your eyes, and do not cover the treated area with a bandage or apply local heat, like heating pads. Following these guidelines will help ensure your safety while using this medication.

Side Effects

When using this product, it's important to apply it only as directed and avoid using it on large areas of your body, on cuts, irritated skin, or puncture wounds. You should not use it for more than one week without consulting a doctor. Be careful to keep it away from your eyes, and do not apply heat or bandage the area where you use it.

If your condition worsens, if symptoms last longer than seven days, or if they improve and then return within a few days, stop using the product and consult a doctor. Additionally, if you are pregnant or breastfeeding, it's best to speak with a healthcare professional before using it. If the product is swallowed, seek medical help or contact Poison Control immediately.

Warnings and Precautions

This product is for external use only, so please avoid applying it to large areas of your body or on any cut, irritated, or swollen skin. It should not be used on puncture wounds, and you should not use it for more than one week without consulting your doctor. Always follow the directions on the packaging carefully, and be sure to keep it away from your eyes. Additionally, do not cover the treated area with bandages or apply heat, like heating pads.

If your condition worsens, if symptoms last longer than seven days, or if they improve and then return within a few days, stop using the product and consult your doctor. If you are pregnant or breastfeeding, it's important to speak with a healthcare professional before using this product.

In case of accidental swallowing, seek emergency medical help or contact the Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it's important to act quickly. You should seek medical help immediately or contact the Poison Control Center for guidance.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to get help. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

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 using this medication for your child, it's important to know that you should consult a doctor if your child is under 12 years old. For children aged 12 and older, you can apply a thin layer of the medication to the affected area every 6 to 8 hours. However, be sure not to exceed three applications in a 24-hour period to ensure safety and effectiveness. Always follow these guidelines to help keep your child safe while using this treatment.

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, it’s important to consult with a healthcare provider for personalized advice. 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 to ensure safe and effective treatment.

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 should be used if you have 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 health situation. They can help determine the best course of action based on your kidney function and overall health.

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 (issues with liver function).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

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 at a controlled room temperature between 20° and 25°C (68° and 77°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, make sure to do so in a clean environment to avoid contamination. Always follow any specific instructions provided with the product for safe use and disposal. Keeping these guidelines in mind will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is RUGBY?

RUGBY is a pain-relieving cream that contains a maximum strength of 4% Lidocaine.

What does RUGBY do?

It temporarily relieves minor pain.

How should I use RUGBY?

For adults and children over 12 years, apply a thin layer to the affected area every 6 to 8 hours, not exceeding 3 applications in a 24-hour period.

Can children under 12 use RUGBY?

Children under 12 years should ask a doctor before use.

Are there any contraindications for RUGBY?

No specific contraindications are mentioned in the provided text.

What should I avoid while using RUGBY?

Do not use on large areas of the body, on cut or irritated skin, or for more than one week without consulting a doctor. Avoid contact with the eyes and do not bandage or apply local heat to the area of use.

What should I do if my condition worsens while using RUGBY?

Stop use and ask a doctor if your condition worsens or if symptoms persist for more than 7 days.

Is RUGBY safe to use during pregnancy or breastfeeding?

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

What should I do if I accidentally swallow RUGBY?

Get medical help or contact Poison Control Center right away if swallowed.

What is the storage condition for RUGBY?

Store RUGBY at controlled room temperature between 20°-25°C (68°-77°F).

Packaging Info

Below are the non-prescription pack sizes of Rugby Lidocaine (lidocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Rugby Lidocaine.
Details

Drug Information (PDF)

This file contains official product information for Rugby Lidocaine, 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 minor 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. The total number of applications must not exceed 3 times within a 24-hour period.

For children under 12 years of age, it is recommended to consult a physician prior to use.

Contraindications

Use is contraindicated in the following situations:

Application on large areas of the body, or on cut, irritated, or swollen skin is not recommended due to the potential for increased absorption and adverse effects. The product should not be applied to puncture wounds to prevent complications. Prolonged use beyond one week without medical consultation is contraindicated to avoid potential risks associated with extended exposure. Contact with the eyes must be avoided to prevent irritation or injury. Additionally, bandaging or applying local heat, such as heating pads, to the area of use is contraindicated as it may enhance absorption and lead to adverse reactions.

Warnings and Precautions

For external use only. This product is contraindicated for application on large areas of the body, as well as on cut, irritated, or swollen skin. It should not be used on puncture wounds and should not be applied for more than one week without prior consultation with a healthcare professional.

When utilizing this product, it is imperative to adhere strictly to the provided directions. Users must read and follow all instructions and warnings indicated on the packaging. Care should be taken to avoid contact with the eyes. Additionally, the area of application should not be bandaged or subjected to local heat, such as heating pads.

Patients are advised to discontinue use and seek medical advice if the condition worsens, if symptoms persist beyond seven days, or if symptoms resolve and then recur within a few days. Pregnant or breastfeeding individuals should consult a healthcare professional before using this product.

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

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.

While using this product, it is essential to adhere strictly to the provided directions and warnings. Patients should avoid contact with the eyes and refrain from bandaging or applying local heat, such as heating pads, to the area of use.

Patients are advised to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than seven days, or if symptoms clear up and then recur within a few days. Additionally, pregnant or breastfeeding individuals should seek advice from a healthcare professional before using this product.

In the event of accidental ingestion, patients should seek medical assistance or contact a Poison Control Center immediately.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 Rugby Lidocaine (lidocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Rugby Lidocaine.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a healthcare professional before use. For adolescents aged 12 years and older, the recommended dosage is to apply a thin layer to the affected area every 6 to 8 hours, with a maximum of 3 applications within a 24-hour period.

Geriatric Use

There is no specific information available 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 a healthcare provider 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 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 administering this medication to lactating individuals.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the drug insert text 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 lack of specific guidance necessitates careful clinical judgment and monitoring of these patients.

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 the 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, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

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

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

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

Patients should be informed not to use the medication on large areas of the body or on cut, irritated, or swollen skin, and it should not be applied to puncture wounds. Emphasize the importance of using the medication only as directed, and encourage patients to read and follow all directions and warnings provided on the carton.

It is crucial to inform patients to avoid contact with the eyes and to refrain from bandaging or applying local heat, such as heating pads, to the area of use. Patients should be advised to stop using the medication and consult a doctor if their condition worsens or if symptoms persist for more than seven days, or if symptoms clear up and then recur within a few days.

For patients who are pregnant or breastfeeding, it is important to recommend that they consult a health professional before using the medication. Additionally, patients should be cautioned against using the medication for more than one week without first consulting a doctor.

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 a controlled room temperature, maintaining a range of 20° to 25°C (68° to 77°F). Proper storage conditions are crucial to ensure the integrity and efficacy of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Rugby Lidocaine, 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 Rugby Lidocaine, 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.