Symptom checker
Select audience type

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

ADD CONDITION

items per page

Solstice Pain Relieving

Last content change checked dailysee data sync status

Active ingredients
  • Camphor (synthetic) 3.1 g/100 g
  • Menthol 6 g/100 g
  • Methyl Salicylate 10 g/100 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2019
Label revision date
November 10, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 3.1 g/100 g
  • Menthol 6 g/100 g
  • Methyl Salicylate 10 g/100 g
Other brand names
Dosage form
Patch
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 2019
Label revision date
November 10, 2025
Manufacturer
MADISON ONE ACME INC
Registration number
M017
NDC root
55614-210
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (3 NDCs)
Packaging & NDC Codes (3)

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

The Solstice Pain Relieving Patch is a topical treatment designed to provide temporary relief from minor aches and pains in muscles and joints. It contains active ingredients such as camphor (3.1%), menthol (6.0%), and methyl salicylate (10%), which work together to soothe discomfort associated with conditions like simple backache, arthritis, strains, bruises, and sprains.

Each patch measures 2.83 inches by 1.81 inches and comes in a box containing 20 patches. This convenient format allows you to apply the patch directly to the affected area for targeted relief.

Uses

If you're dealing with minor aches and pains in your muscles and joints, this medication can help provide temporary relief. It's effective for various conditions, including simple backaches, arthritis, strains, bruises, and sprains.

You can rely on it to ease discomfort from these common issues, allowing you to get back to your daily activities with less pain. Remember, while it can help with these specific types of pain, it's always a good idea to consult with a healthcare professional if you have any concerns or if your symptoms persist.

Dosage and Administration

To use this medication effectively, start by cleaning and drying the area of your skin that needs treatment. Once the area is ready, carefully remove the protective film from the patch. You can then apply the patch to the affected area, but make sure not to use it more than 3 to 4 times in a single day. Each patch should be removed after a maximum of 8 hours. To make removal easier, wet the patch with warm water before taking it off.

If you are using this medication for a child under 3 years old, it’s important to consult your physician for guidance.

What to Avoid

You should avoid using this product on irritated or damaged skin, especially over wounds. It's important to keep it away from your eyes and mucous membranes to prevent irritation. When applying, do not bandage tightly, as this can cause complications. Additionally, avoid using heat sources like heating pads or hot water bottles on the area, as this can significantly increase the risk of serious burns. Lastly, steer clear of applying it to very hairy areas of skin to minimize discomfort when removing the patch.

Side Effects

You should be aware that this product is for external use only. If your condition worsens, symptoms last longer than 7 days, or if they clear up and then return within a few days, it's important to stop using the product and consult a doctor. Additionally, if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, seek medical advice.

If you feel actual pain, blistering, or burning after applying the product (a warming or cooling sensation is normal), or if you're using it for arthritis pain and it persists for more than 10 days, or if you notice redness, you should also contact a healthcare professional. This is especially important for children under 12 years of age.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any irritated or damaged skin, including open wounds. If you accidentally swallow the product, seek medical help or contact a Poison Control Center immediately.

You should stop using the product and call your doctor if your condition worsens, if symptoms last longer than 7 days, or if symptoms improve and then return within a few days. Additionally, seek medical advice if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, a skin rash, or if you feel pain, blistering, or burning after application (a warming or cooling sensation is normal). If you are using this product for arthritis pain, contact your doctor if the pain lasts more than 10 days, if you notice redness, or if it’s being used on a child under 12 years old.

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 is crucial to seek immediate medical attention.

In case of an emergency, you should call your local emergency services or go to the nearest hospital. Always keep your medications in a safe place 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 planning to become pregnant, it's important to be cautious with any medications or products you use. You should avoid using this product on irritated or damaged skin, especially on wounds. Before using it, consult with your doctor or pharmacist if you have any concerns.

If you experience nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash while using this product, stop using it immediately and seek medical advice. Additionally, if you have children under 3 years of age, please consult your physician before use. Your health and the health of your baby are paramount, so always prioritize safety and communication with your healthcare provider.

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 is no information available about whether this product is excreted in breast milk or any potential risks it may pose to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If you have a child under 3 years old, it's important to consult your physician before using this medication. For children under 12 years old, special precautions should be taken if the medication is being used to treat arthritis pain. Always ensure you discuss any concerns or questions with your child's healthcare provider to ensure their safety and well-being.

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 to ensure safe and effective treatment.

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 or how it should be managed in the context of liver impairment.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific health needs. They can help you understand how your liver condition may interact with medications and what steps to take for your health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual’s health situation is unique, and your provider can help ensure that your treatment plan is safe and effective for you. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

Storage and Handling

To ensure the best performance of your patches, store them in their zip-lock pouch and keep it tightly closed. This helps protect the patches from moisture and contamination. It's also important to avoid exposing them to excessive heat, as high temperatures can affect their effectiveness.

When handling the patches, always make sure your hands are clean to maintain their safety and integrity. Following these simple guidelines will help you use the patches effectively and safely.

Additional Information

You should apply the patch to the affected area of your skin no more than 3 to 4 times a day, and remember to remove it after a maximum of 8 hours. It's important to keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately. Additionally, if you experience any unexpected side effects while using this product, please report them to the FDA MedWatch Program.

FAQ

What is the Solstice Pain Relieving Patch used for?

The Solstice Pain Relieving Patch is used for the temporary relief of minor aches and pains of muscles and joints due to conditions like simple backache, arthritis, strains, bruises, and sprains.

How should I apply the patch?

Clean and dry the affected area, remove the protective film from the patch, and apply it not more than 3 to 4 times daily. Remove the patch after a maximum of 8 hours.

Are there any contraindications for using this patch?

Do not use the patch on irritated or damaged skin or on wounds, and avoid contact with the eyes or mucous membranes.

What should I do if I experience side effects?

Stop use and ask a doctor if you experience nausea, vomiting, abdominal discomfort, diarrhea, skin rash, or if your condition worsens or persists for more than 7 days.

Is it safe to use the patch on children?

Consult your physician before using the patch on children under 3 years of age, and special precautions are advised for children under 12 years of age.

What should I do if the patch is swallowed?

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

Can I use the patch if I am pregnant or nursing?

There are no specific warnings or recommendations regarding the use of this product in pregnant or nursing mothers.

How should I store the patches?

Keep the patches tightly closed in the zip-lock pouch and avoid excessive heat.

Packaging Info

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

Packaging configurations for Solstice Pain Relieving.
Details

Drug Information (PDF)

This file contains official product information for Solstice Pain Relieving, 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 aches and pains associated with muscles and joints. Specifically, it is effective for conditions such as 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 aged 3 years and older, the affected area should be cleaned and dried prior to application. The protective film from the patch must be removed before placing the patch on the affected area. The patch may be applied up to 3 to 4 times daily, ensuring that each application does not exceed 8 hours. To facilitate removal, the patch should be wetted with warm water before detaching it from the skin.

For children under 3 years of age, it is recommended to consult a physician for appropriate guidance.

Contraindications

Use is contraindicated in the following situations:

Application on irritated or damaged skin, including wounds, is prohibited due to the potential for exacerbating the condition. Contact with the eyes or mucous membranes must be avoided to prevent irritation or injury. Tight bandaging of the application site is not recommended, as it may lead to compromised circulation. The application of heat, such as heating pads, hot water bottles, or lamps, is contraindicated due to an increased risk of serious burns. Additionally, placement on extremely hairy areas of skin should be avoided to minimize irritation during patch removal.

Warnings and Precautions

For external use only. This product is contraindicated for application on irritated or damaged skin, including open wounds, to prevent exacerbation of the condition.

Healthcare professionals should advise patients to seek emergency medical assistance or contact a Poison Control Center immediately if the product is ingested.

Patients are instructed to discontinue use and consult a physician under the following circumstances:

  • If the condition worsens or symptoms persist beyond 7 days.

  • If symptoms resolve and then recur within a few days.

  • If excessive skin irritation develops.

  • If gastrointestinal symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occur.

  • If the patient experiences actual pain, blistering, or burning following application, noting that a warming or cooling sensation is expected.

  • In cases of arthritis pain, if discomfort persists for more than 10 days, if redness is observed, or if the product is being used for children under 12 years of age.

Regular monitoring of the patient's response to treatment is recommended to ensure safety and efficacy.

Side Effects

Patients using this product should be aware that it is intended for external use only. In clinical practice, participants have reported various adverse reactions, which can be categorized based on seriousness and frequency.

Serious adverse reactions warrant immediate medical attention. Patients should stop using the product and consult a healthcare professional if they experience any of the following: worsening of their condition, persistence of symptoms beyond 7 days, recurrence of symptoms after they have cleared, excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or the development of a skin rash. Additionally, if patients experience actual pain, blistering, or burning after application—beyond the expected warming or cooling sensation—they should seek medical advice.

For patients using the product for arthritis-related pain, it is crucial to discontinue use and consult a doctor if pain persists for more than 10 days, if redness is present, or if the product is being used on children under 12 years of age. These precautions are essential to ensure patient safety and to address any potential complications associated with the use of this product.

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 Solstice Pain Relieving (camphor, menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Solstice Pain Relieving.
Details

Pediatric Use

Pediatric patients under 3 years of age should consult a physician prior to use. For children under 12 years of age, special precautions are advised when administering this medication for the treatment of arthritis-related pain. It is essential for healthcare professionals to consider these age-specific recommendations to ensure safe and effective use in the pediatric population.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

Pregnant patients should exercise caution when considering the use of this product. It is advised that they do not apply it to irritated or damaged skin, including wounds. Prior to use, pregnant patients are encouraged to consult with a healthcare professional, such as a doctor or pharmacist, to address any concerns regarding the safety and appropriateness of this product during pregnancy.

In the event that adverse reactions occur, such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash, pregnant patients should discontinue use and seek medical advice promptly. Additionally, this product is not recommended for children under 3 years of age; therefore, consultation with a physician is necessary for this population.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no specific information regarding renal impairment, dosage adjustments, special monitoring, or safety considerations for patients with reduced kidney function. Healthcare professionals should exercise caution and consider individual patient factors when treating patients with renal impairment, as the absence of detailed guidance necessitates careful clinical judgment.

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, remain observant for potential overdose symptoms, and implement appropriate management strategies as needed.

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

Reports of unexpected side effects associated with the use of this product have been received through voluntary submissions and surveillance programs. Healthcare professionals and consumers are encouraged to report any adverse events to the FDA MedWatch Program. Serious side effects can also be reported directly by calling 888-221-3496, available Monday through Friday from 9 am to 5 pm.

Patient Counseling

Patients should be advised to keep this product out of reach of children. In the event of accidental ingestion, they should seek medical assistance or contact a Poison Control Center immediately.

It is important to inform patients that this product should not be applied to irritated or damaged skin, including open wounds. Patients should be instructed to discontinue use and consult a healthcare provider if any of the following occur: the condition worsens, symptoms persist for more than 7 days, symptoms resolve and then recur within a few days, excessive skin irritation develops, or if they experience nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash. Additionally, patients should seek medical advice if they feel actual pain or experience blistering or burning after application, noting that a warming or cooling sensation is expected.

For patients using this product for arthritis pain, they should be informed to stop use and consult a doctor if pain persists for more than 10 days, if redness is present, or if the product is being used on children under 12 years of age.

While using this product, patients should be cautioned to avoid contact with the eyes and mucous membranes. They should not bandage the area tightly or apply heat, such as heating pads, hot water bottles, or lamps, as this may increase the risk of serious burns. Patients should also avoid applying the product to extremely hairy areas of skin to prevent irritation during patch removal.

Finally, patients are encouraged to consult with a doctor or pharmacist if they have any concerns regarding the use of this product.

Storage and Handling

Patches are supplied in a zip-lock pouch, which must be kept tightly closed to maintain product integrity. It is essential to store the patches in a cool, dry place, avoiding exposure to excessive heat to ensure optimal performance and longevity.

Additional Clinical Information

The product is administered topically, with patches applied to the affected area no more than 3 to 4 times daily. Each patch should be removed after a maximum application time of 8 hours. Clinicians should advise patients to report any unexpected side effects to the FDA MedWatch Program. Additionally, it is crucial to keep the product out of reach of children; if ingested, medical assistance or contact with a Poison Control Center is recommended.

Drug Information (PDF)

This file contains official product information for Solstice Pain Relieving, 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 Solstice Pain Relieving, 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.