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Sync Pro

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Active ingredients
  • Camphor (synthetic) 4 g
  • Menthol 10 g
  • Methyl Salicylate 30 g
Other brand names
Dosage form
Cream
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
July 28, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 4 g
  • Menthol 10 g
  • Methyl Salicylate 30 g
Other brand names
Dosage form
Cream
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
July 28, 2025
Manufacturer
iON Pharma, LLC
Registration number
M017
NDC root
82944-400
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

syn relief PRO is a topical analgesic cream designed to provide long-lasting relief from minor aches and pains in your muscles and joints. It is particularly effective for conditions such as simple backache, arthritis, strains, bruises, and sprains. The cream has a light scent and is intended for external use only, making it a convenient option for managing discomfort in various areas of your body.

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 aches and pains, it's always a good idea to consult with a healthcare professional if you have any concerns.

Dosage and Administration

It's important to use this medication only as directed by your healthcare provider. If you are an adult or a child aged 12 years and older, you can apply it to the affected area up to 3 to 4 times a day. Make sure to follow the recommended frequency to ensure safety and effectiveness.

If the patient is a child under 12 years old, it's best to consult a doctor before use. They can provide guidance on the appropriate dosage and application for younger patients. Always prioritize safety and follow the advice of a healthcare professional.

What to Avoid

It's important to use this medication safely. You should avoid contact with your eyes or any mucous membranes, as this can lead to irritation or other issues. Additionally, do not bandage the area tightly, as this could cause complications.

There are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. However, following these guidelines will help ensure your safety and the effectiveness of your treatment.

Side Effects

You should be aware of some important information regarding potential side effects. If you notice that your condition worsens or symptoms last longer than 7 days, it's essential to stop using the product and consult a doctor. Additionally, if your symptoms improve but then return within a few days, or if you experience excessive skin irritation, you should also seek medical advice.

It's important to avoid using this product on wounds or damaged skin, and it should not be used with a heating pad. Furthermore, it is not recommended for children under 12 years of age who have arthritis-like conditions.

Warnings and Precautions

It's important to use this medication safely. Avoid applying it to any wounds or damaged skin, and do not use it with a heating pad. If you are considering this treatment for a child under 12 years old who has arthritis-like conditions, please refrain from using it.

If you accidentally swallow the medication, seek emergency medical help or contact a Poison Control Center immediately. You should also stop using the medication and call your doctor if your condition worsens, if symptoms last longer than 7 days, if symptoms improve and then return within a few days, or if you experience excessive skin irritation.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include extreme drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your safety and health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this medication during pregnancy has not been established. It is not recommended for use while you are pregnant because there may be potential risks to your developing baby. Always consult with your healthcare provider to discuss any medications you are considering and to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into your breast milk, and the effects on nursing infants have not been thoroughly studied. Therefore, exercising caution is recommended to ensure the safety and well-being of your baby.

Pediatric Use

If your child is under 12 years old and has arthritis-like conditions, it's important not to use this medication. For children in this age group, you should consult a doctor before use.

For those aged 12 and older, you can apply the medication to the affected area, but be sure to limit applications to no more than 3 to 4 times a day. Always follow your healthcare provider's guidance to ensure safe and effective use.

Geriatric Use

When considering the use of Sync Relief Pro Cream for older adults, it's important to note that the drug insert does not provide specific information about how this product may affect elderly patients. This means there are no special dosage adjustments, safety concerns, or precautions outlined for older individuals.

As a caregiver or an older adult, you should always consult with a healthcare professional before starting any new treatment. They can help determine if this cream is appropriate for you, taking into account your unique health needs and any other medications you may be using.

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 determine the best approach for managing your health, especially if you have concerns about your kidneys.

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 discuss any concerns you may have regarding your liver function and how it relates to your treatment. They can help ensure that your medication is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that this medication is generally considered safe to use alongside other treatments and tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions or express any concerns you may have regarding your medications or tests.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Once you open the product, be sure to discard it after use to maintain safety and quality. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

For adults and children aged 12 years and older, you should apply the medication to the affected area no more than 3 to 4 times a day. If the patient is under 12 years old, it's important to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is syn relief PRO?

Syn relief PRO is a topical analgesic cream designed for pain relief, providing long-lasting relief for minor aches and pains of muscles and joints.

What conditions does syn relief PRO help with?

It temporarily relieves minor aches and pains associated with simple backache, arthritis, strains, bruises, and sprains.

How should I use syn relief PRO?

Apply syn relief PRO to the affected area not more than 3 to 4 times daily for adults and children 12 years and older. For children under 12, consult a doctor.

Are there any warnings for using syn relief PRO?

Do not use on wounds or damaged skin, with a heating pad, or on children under 12 with arthritis-like conditions. Avoid contact with eyes or mucous membranes.

What should I do if my condition worsens?

Stop use and consult a doctor if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation occurs.

Is syn relief PRO safe to use during pregnancy?

Safety during pregnancy has not been established, and it is not recommended for use due to potential risks to the fetus.

Can nursing mothers use syn relief PRO?

Nursing mothers should consult a healthcare professional before using this product, as there is a potential for excretion in breast milk.

How should I store syn relief PRO?

Store at room temperature, protect from light, and do not freeze. Discard after opening.

Packaging Info

Below are the non-prescription pack sizes of Sync Pro (sync relief pro cream). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sync Pro.
Details

Drug Information (PDF)

This file contains official product information for Sync Pro, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

NDC 82944-400-10, syn relief PRO is a topical analgesic formulated as a pain relief cream. It is designed for external use only and provides long-lasting relief from pain. The product has a light scent and is packaged in a net weight of 4 oz (113 g).

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

The medication should be used only as directed. For adults and children aged 12 years and older, it is recommended to apply the product to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a physician before use.

Contraindications

Use of this product is contraindicated in the following situations:

Contact with eyes or mucous membranes should be avoided due to the potential for irritation or adverse reactions. Additionally, tight bandaging is contraindicated as it may lead to compromised circulation or other complications.

Warnings and Precautions

The use of this product requires careful consideration of specific warnings and precautions to ensure patient safety and efficacy.

Contraindications for Use This product should not be applied to wounds or damaged skin, as this may exacerbate the condition or lead to further complications. Additionally, it is contraindicated for use with heating pads, which may increase the risk of adverse effects. The product is not recommended for children under 12 years of age who present with arthritis-like conditions.

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

Monitoring and Discontinuation Patients should be advised to discontinue use and consult a healthcare professional if any of the following occur: the condition worsens or symptoms persist beyond 7 days; symptoms resolve only to reappear within a few days; or if excessive skin irritation develops. Regular monitoring of the patient's response to treatment is essential to ensure safety and effectiveness.

Side Effects

Patients should be aware of the following adverse reactions associated with the use of this product.

Serious adverse reactions include the potential for excessive skin irritation. In such cases, patients are advised to discontinue use and consult a healthcare professional. Additionally, the product should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad. It is also contraindicated for use in children under 12 years of age who present with arthritis-like conditions.

Patients are encouraged to stop use and seek medical advice if their condition worsens or if symptoms persist for more than 7 days. Furthermore, if symptoms resolve and then recur within a few days, or if excessive skin irritation occurs, it is imperative to consult a healthcare provider.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Sync Pro (sync relief pro cream). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sync Pro.
Details

Pediatric Use

Pediatric patients under 12 years of age with arthritis-like conditions should not use this medication. For children in this age group, it is advised to consult a healthcare professional before use.

For adolescents aged 12 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

There is no specific information regarding the use of Sync Relief Pro Cream in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as the absence of data necessitates careful consideration of individual patient factors and potential risks. Monitoring for any adverse effects or unusual responses in this population is advisable, given the lack of established guidelines for geriatric use.

Pregnancy

Safety during pregnancy has not been established for this medication. It is not recommended for use during pregnancy due to potential risks to the fetus. Healthcare professionals should consider the potential risks and benefits when prescribing this medication to pregnant patients or women of childbearing potential.

Lactation

Nursing mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk, and the effects on nursing infants are not well studied; therefore, caution is advised.

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 clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the substance involved, estimated dose, and time of exposure, is crucial for effective management and follow-up care.

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

No postmarketing experience details are available in the insert text.

Patient Counseling

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

Patients should be informed to stop using the product and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, they should be aware that if symptoms clear up and then recur within a few days, they should also seek medical advice. Patients must be cautioned to discontinue use and consult a healthcare professional if they experience excessive skin irritation.

While using this product, patients should be instructed to avoid contact with their eyes or mucous membranes. It is also important to inform them not to bandage the area tightly to ensure proper application and minimize the risk of adverse effects.

Storage and Handling

The product is supplied in configurations that include specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Once opened, the product must be discarded to ensure safety and efficacy.

Additional Clinical Information

For adults and children aged 12 years and older, the medication should be applied to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a doctor regarding the appropriate use. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Sync Pro, 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 Sync Pro, 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.