Symptom checker
Select audience type

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

ADD CONDITION

items per page

Paingel

Last content change checked dailysee data sync status

Active ingredients
  • Menthol 7 g/100 mL
  • Methyl Salicylate 20 g/100 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
February 18, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol 7 g/100 mL
  • Methyl Salicylate 20 g/100 mL
Other brand names
Dosage form
Spray
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 2025
Label revision date
February 18, 2026
Manufacturer
NACOR BUSINESS GROUP LLC
Registration number
M017
NDC root
85110-207
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

PAINGEL SPRAY is a topical medication designed to provide temporary relief from minor aches and pains in muscles and joints. It is commonly used for conditions such as simple backache, arthritis, strains, bruises, and sprains. This spray can be a helpful option for managing discomfort associated with everyday activities or injuries.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is effective for conditions such as simple backache, arthritis, strains, bruises, and sprains. If you're dealing with any of these discomforts, this medication may help ease your symptoms.

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 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 spray two to three pumps onto the affected area. You can do this as needed, but make sure not to exceed three to four applications in a single day.

If you have a child under 12 years of age, it’s important not to use this medication without first consulting a doctor. Always follow these guidelines to ensure safe and effective use.

What to Avoid

It's important to follow specific guidelines when using this product to ensure your safety and effectiveness. You should avoid bandaging the area tightly, as this can cause complications. Additionally, make sure to keep the product away from your eyes and mucous membranes, as contact can lead to irritation. Lastly, do not expose the treated area to heat or direct sunlight, as this may affect the treatment.

By adhering to these precautions, you can help ensure a safer experience with the product. If you have any questions or concerns, please consult with a healthcare professional.

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 last more than 7 days. Additionally, if your symptoms improve and then return within a few days, or if you experience signs of injury like pain, swelling, or blistering at the application site, seek medical advice.

Remember, this product is for external use only. Avoid applying it to wounds or damaged skin, using it with a heating pad, or applying it to children under 12 years of age.

Warnings and Precautions

This product is for external use only, so please avoid applying it to wounds or damaged skin. It should not be used with a heating pad or on children under 12 years old.

If you accidentally swallow the product, seek emergency medical help or contact a Poison Control Center immediately.

You should stop using the product and call your doctor if your condition worsens, if you notice redness or irritation, if symptoms last more than 7 days, or if they return shortly after clearing up. Additionally, if you experience any signs of injury, such as pain, swelling, or blistering at the application site, please reach out to your healthcare provider.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's important to be aware of the general signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect that you or someone else may have taken too much of a medication, it’s crucial to seek immediate medical help.

In case of an overdose, you should contact your local emergency services or go to the nearest hospital right away. Always keep the medication packaging on hand, as it can provide important information to healthcare professionals. Remember, it's better to be safe and get checked out if you have any concerns about an overdose.

Pregnancy Use

If you are pregnant or planning to become pregnant, it’s important to consult with a healthcare professional before using this medication. They can provide guidance tailored to your specific situation and help you understand any potential risks. Always prioritize your health and the health of your baby 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 using this product for children. If your child is under 12 years old, you should not use it without consulting a doctor first. Additionally, avoid applying the product to any wounds or damaged skin, and do not use it with a heating pad. Always prioritize your child's safety and seek professional advice if you're unsure.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s wise to discuss any potential risks or benefits 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 regular check-ins with your healthcare team are essential to ensure 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 you understand any necessary precautions or adjustments based on your kidney 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 may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver condition. They can help monitor your health and make any necessary adjustments to your treatment plan.

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 tests you are undergoing. This way, you can avoid any potential issues and receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it in a tightly closed container in a dry location. Keep the temperature between 59°F and 86°F (15°C and 30°C) to maintain its effectiveness.

When handling the product, always ensure that you do so in a clean environment to avoid contamination. If you have any specific disposal instructions, please follow them carefully to ensure safety.

Additional Information

No further information is available.

FAQ

What is PAINGEL SPRAY used for?

PAINGEL SPRAY is used for temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

How should I use PAINGEL SPRAY?

For adults and children over 12 years of age, spray two to three pumps on the affected area not more than three to four times daily. Do not use on children under 12 years of age without consulting a doctor.

Are there any warnings for using PAINGEL SPRAY?

Yes, it is for external use only. Do not apply to wounds or damaged skin, use with a heating pad, or on children under 12 years of age.

What should I do if I experience side effects?

Stop using the spray and consult a doctor if your condition worsens, redness or irritation develops, symptoms persist for more than 7 days, or you notice signs of injury like pain or swelling.

Can I use PAINGEL SPRAY if I am pregnant or breastfeeding?

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

What should I avoid while using PAINGEL SPRAY?

Avoid contact with eyes and mucous membranes, do not bandage tightly, and do not expose the treated area to heat or direct sunlight.

What should I do if PAINGEL SPRAY is swallowed?

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

How should I store PAINGEL SPRAY?

Store PAINGEL SPRAY tightly closed in a dry place at controlled room temperature between 59°F - 86°F (15°C - 30°C).

Packaging Info

Below are the non-prescription pack sizes of Paingel (menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Paingel.
Details

Drug Information (PDF)

This file contains official product information for Paingel, 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 specified drug.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

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

Dosage and Administration

For adults and children over 12 years of age, the recommended dosage is to spray two to three pumps onto the affected area as necessary, not exceeding three to four applications per day.

In children under 12 years of age, the product is not recommended for use. Consultation with a healthcare professional is advised prior to administration in this age group.

Contraindications

Use of this product is contraindicated in the following situations:

Tight bandaging should be avoided, as it may lead to compromised circulation. Contact with eyes and mucous membranes must be strictly avoided to prevent irritation or injury. Additionally, exposure of the treated area to heat or direct sunlight is contraindicated due to the potential for adverse reactions or diminished efficacy of the product.

Warnings and Precautions

The product is intended for external use only and should not be applied to wounds or damaged skin. It is contraindicated for use with a heating pad and is not recommended for children under 12 years of age.

In the event of accidental ingestion, immediate medical assistance should be sought. Contact a Poison Control Center or seek emergency medical help without delay.

Healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: worsening of the condition, presence of redness, development of irritation, persistence of symptoms beyond 7 days, or recurrence of symptoms shortly after resolution. Additionally, patients should seek medical attention if they experience signs of injury, such as pain, swelling, or blistering at the site of application.

Side Effects

Patients using this product may experience various adverse reactions. It is important to note that the product is intended for external use only and should not be applied to wounds or damaged skin. Additionally, it should not be used in children under 12 years of age.

In the event that a patient's condition worsens, or if redness, irritation, or any other concerning symptoms develop, it is advised to stop use and consult a healthcare professional. Patients should also seek medical advice if symptoms persist for more than 7 days, if they resolve and then recur within a few days, or if they experience signs of injury, such as pain, swelling, or blistering at the site of application.

These precautions are essential to ensure the safe use of the product and to mitigate the risk of serious adverse reactions.

Drug Interactions

There are currently no documented drug interactions associated with 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 Paingel (menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Paingel.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this product. It is important to consult a doctor for any concerns regarding its use in this age group. Additionally, the product should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad.

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, given the lack of targeted data for this population.

Pregnancy

Pregnant patients 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 are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure the safety of both the mother and the developing fetus.

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 available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

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

There is currently no specific information available regarding overdosage for this medication. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Continuous monitoring of vital signs and clinical status is essential. If symptoms of overdosage are observed, appropriate interventions should be implemented based on the patient's condition.

Healthcare professionals should also consider contacting a poison control center or a medical toxicologist for guidance on management strategies tailored to the specific situation. It is crucial to document any overdosage incidents thoroughly and report them to the relevant regulatory authorities as part of ongoing pharmacovigilance efforts.

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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important to instruct patients to stop using the product and consult a doctor if any of the following occur: the condition worsens, redness develops, irritation occurs, symptoms persist for more than 7 days, or if symptoms clear up only to return within a few days. Patients should also be informed to seek medical attention if they experience signs of injury, such as pain, swelling, or blistering at the site of application.

Patients must be reminded to use the product only as directed and to avoid tightly bandaging the treated area. They should be cautioned against contact with the eyes and mucous membranes. In the event of an allergic reaction, patients should discontinue use immediately and consult a healthcare professional. Additionally, it is essential to advise patients not to expose the treated area to heat or direct sunlight.

Storage and Handling

The product is supplied in a tightly closed container to ensure stability and integrity. It should be stored in a dry place at controlled room temperature, specifically between 59°F and 86°F (15°C and 30°C). Proper storage conditions are essential to maintain the product's efficacy and safety.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Paingel, 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 Paingel, 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.