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Neuracin Topical Gel

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Active ingredients
  • Menthol, Unspecified Form 100 mg/1 g
  • Camphor (synthetic) 40 mg/1 g
  • Methyl Salicylate 300 mg/1 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2021
Label revision date
December 8, 2025
Active ingredients
  • Menthol, Unspecified Form 100 mg/1 g
  • Camphor (synthetic) 40 mg/1 g
  • Methyl Salicylate 300 mg/1 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2021
Label revision date
December 8, 2025
Manufacturer
SOLA Pharmaceuticals
Registration number
M017
NDC root
70512-104

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Drug Overview

Neuracin Topical Analgesic Gel is a medication designed to provide temporary relief from minor pain. It is commonly used for conditions such as arthritis, simple backache, muscle strains, bruises, and muscle sprains. By applying this gel to the affected area, you can help alleviate discomfort and improve your mobility.

This 2oz (56.7g) gel works by targeting the pain directly at the site of application, making it a convenient option for managing everyday aches and pains. If you have any questions or need further information, feel free to reach out for assistance.

Uses

You can use this medication to temporarily relieve minor pain from various conditions. If you're dealing with arthritis, simple backaches, muscle strains, bruises, or muscle sprains, this medication may help ease your discomfort.

It's important to note that the information provided indicates there are no teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects mentioned. This makes it a safer option for those concerned about these specific risks.

Dosage and Administration

You should apply the medication directly to the affected area, making sure not to use it more than 3 to 4 times a day. This helps ensure that you get the best results without overusing the product.

If you are considering this medication for a child under 12 years old, it’s important to consult a doctor first. They can provide guidance on the appropriate use and dosage for younger patients.

What to Avoid

It's important to be aware of certain precautions when using this medication. If you accidentally swallow it, seek medical help immediately. Additionally, if you are pregnant or breastfeeding, please consult with a healthcare professional before using this product to ensure it is safe for you and your baby.

While there are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication, it's always best to use it responsibly and under the guidance of a healthcare provider. Your safety is the top priority.

Side Effects

When using this product, it's important to remember that it is for external use only. You should avoid contact with your eyes and mucous membranes, and do not apply it to wounds or damaged skin. Additionally, refrain from tightly bandaging the area or using a heating pad while using this product. Always follow the directions provided.

If your condition worsens, lasts more than 7 days, or clears up only to return within a few days, stop using the product and consult your doctor.

Warnings and Precautions

This product is for external use only, so please avoid contact with your eyes and mucous membranes. Do not apply it to any wounds or damaged skin, and refrain from tightly bandaging the area or using it with a heating pad. Always use the product as directed.

If your condition worsens, or if your symptoms last more than 7 days or improve and then return within a few days, stop using the product and consult your doctor. Additionally, if the product is swallowed, seek emergency medical help immediately.

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 an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, call your local emergency services or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

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 have a child under 12 years old, it's important to consult a doctor before using this medication. This ensures that the treatment is safe and appropriate for your child's specific needs. Always prioritize professional guidance when it comes to the health of your little ones.

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, be sure to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach, considering any unique health needs or conditions that may be present. Always prioritize safety and open communication when it comes to managing health in later years.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

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 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 and safety of your product, store it at a temperature between 20-25ºC (68-77ºF). It's important to keep it away from heat sources, as excessive heat can affect its quality.

When handling the product, always do so with care to maintain its integrity. Make sure to follow any additional safety guidelines provided with the product to ensure safe usage and disposal.

Additional Information

No further information is available.

FAQ

What is Neuracin Topical Analgesic Gel used for?

Neuracin Topical Analgesic Gel temporarily relieves minor pain associated with arthritis, simple backache, muscle strains, bruises, and muscle sprains.

How should I use Neuracin Topical Analgesic Gel?

Apply Neuracin on the affected area no more than 3 to 4 times daily. Avoid contact with eyes and mucous membranes, and do not apply to wounds or damaged skin.

Are there any warnings I should be aware of?

Yes, Neuracin is for external use only. Do not bandage tightly or use with a heating pad, and stop use if your condition worsens or symptoms last more than 7 days.

What should I do if I swallow Neuracin?

If swallowed, get medical help right away.

Can I use Neuracin if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, consult a health professional before using Neuracin.

Is Neuracin safe for children?

Children under 12 years of age should consult a doctor before using Neuracin.

How should I store Neuracin?

Store Neuracin at 20-25ºC (68-77ºF) and away from heat.

What should I do if my symptoms return after using Neuracin?

If your symptoms clear up and then occur again within a few days, stop use and ask a doctor.

Packaging Info

Below are the non-prescription pack sizes of Neuracin Topical Gel (neuracin topical analgesic gel). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Neuracin Topical Gel.
Details

Drug Information (PDF)

This file contains official product information for Neuracin Topical Gel, 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 associated with various conditions, including arthritis, simple backache, muscle strains, bruises, and muscle sprains.

There are no teratogenic or nonteratogenic effects associated with this drug as per the available data.

Dosage and Administration

The medication should be applied to the affected area, with a maximum frequency of 3 to 4 times daily. For patients under 12 years of age, it is essential to consult a healthcare professional prior to use to ensure safety and appropriateness of treatment.

Contraindications

Use is contraindicated in individuals who are pregnant or breastfeeding without prior consultation with a healthcare professional. In the event of accidental ingestion, immediate medical assistance should be sought.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to avoid contact with the eyes and mucous membranes when using this product. It is imperative that the product is not applied to wounds or damaged skin. Additionally, patients should be cautioned against tightly bandaging the area of application or using the product in conjunction with a heating pad. The product should be used strictly as directed to ensure safety and efficacy.

Patients are instructed to discontinue use and consult a healthcare provider if their 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, immediate medical assistance should be sought.

Side Effects

Patients using this product should be aware that it is for external use only. It is crucial to avoid contact with the eyes and mucous membranes, and the product should not be applied to wounds or damaged skin. Additionally, patients are advised not to bandage the area tightly or use it in conjunction with a heating pad. The product should be used strictly as directed.

In the event that the condition worsens, or if symptoms persist for more than 7 days or resolve and then recur within a few days, patients should discontinue use and consult a healthcare professional.

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 Neuracin Topical Gel (neuracin topical analgesic gel). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Neuracin Topical Gel.
Details

Pediatric Use

Pediatric patients under 12 years of age should be evaluated by a healthcare professional prior to use. It is essential to consult a doctor to determine the appropriate treatment and dosage for this age group.

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 potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

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 weighed, as the effects on fetal outcomes and lactation 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 no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the text. Therefore, healthcare professionals should exercise caution and consider individual patient factors when prescribing to this population. Regular monitoring of renal function may be warranted to ensure safe and effective use of the medication in 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 overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, increased severity of known side effects, unusual behavioral changes, or any other atypical clinical manifestations.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. It is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for specific guidance on the management of overdose cases.

In summary, while specific overdosage information is not available, healthcare professionals should exercise caution, monitor for symptoms, and provide appropriate supportive care in the event of an overdose.

Nonclinical Toxicology

If pregnant or breast-feeding, it is advised to consult a health professional prior to use. No additional information regarding non-teratogenic effects is available in the insert. Furthermore, there is no data provided concerning nonclinical toxicology or animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. In the event that the medication is swallowed, patients should be instructed to seek medical help immediately.

Additionally, it is important for healthcare providers to discuss the use of this medication with patients who are pregnant or breastfeeding. Patients should be encouraged to consult a health professional before using the medication in these circumstances to ensure safety for both themselves and their child.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available upon request. It should be stored at a controlled room temperature of 20-25ºC (68-77ºF). Care should be taken to keep the product away from heat sources to maintain its integrity and efficacy.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Neuracin Topical Gel, 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 Neuracin Topical Gel, 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.