ADD CONDITION

items per page

Barox

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredients
  • Camphor (synthetic) 5.90 g/100 g
  • Menthol 0.80 g/100 g
  • Methyl Salicylate 4.60 g/100 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2017
Label revision date
November 16, 2017
Active ingredients
  • Camphor (synthetic) 5.90 g/100 g
  • Menthol 0.80 g/100 g
  • Methyl Salicylate 4.60 g/100 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 2017
Label revision date
November 16, 2017
Manufacturer
Barox Co. , Ltd.
Registration number
part348
NDC root
55692-150

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

Barox S is an anti-inflammatory pain-relieving ointment that you can apply to your skin. It is designed to help relieve muscle and joint pain associated with conditions like arthritis, rheumatism, backaches, knee pain, and shoulder pain. By targeting inflammation, Barox S aims to provide you with comfort and ease in your daily activities.

Uses

Barox S is a topical ointment designed to help relieve pain and inflammation in your muscles and joints. If you’re dealing with discomfort from conditions like arthritis, rheumatalgia (pain in the muscles and joints), backaches, knee pain, or shoulder pain, this ointment may provide the relief you need.

By applying Barox S to the affected areas, you can experience soothing effects that target your pain directly. It's a convenient option for managing everyday aches and pains associated with these common conditions.

Dosage and Administration

It's important to use this medication exactly as directed by your healthcare provider. If you are an adult or a child aged 12 years and older, you should apply it to the affected area of your skin. Make sure to do this no more than 3 to 4 times each day.

When applying the medication, focus on the specific area that needs treatment. Remember, sticking to the recommended frequency of 3 to 4 times daily is key to ensuring its effectiveness. Always follow the instructions provided to achieve the best results.

What to Avoid

There are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. Additionally, there are no explicit instructions indicating that you should not take or use this medication. Always consult with your healthcare provider for personalized advice and to ensure this medication is appropriate for you.

Side Effects

It's important to use this medication only on the skin and to avoid getting it in your eyes. Make sure to keep it and all other medications out of the reach of children to prevent accidental ingestion or misuse. If you have any concerns about using this product, please consult with a healthcare professional for guidance.

Warnings and Precautions

This product is for external use only, so please avoid getting it in your eyes. It's important to keep this and all medications out of the reach of children to prevent accidental ingestion or misuse.

If you experience any unusual reactions or have concerns while using this product, stop using it immediately and consult your doctor for further guidance. Always prioritize your safety and well-being when using any medication.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contacting your local poison control center or going to the nearest emergency room is crucial. They can provide the necessary guidance and treatment. Always remember that it's better to be safe and get checked if you have any concerns about your health.

Pregnancy Use

When it comes to using this product during pregnancy, there is no specific information available about its safety or potential risks to you or your developing baby. The insert does not indicate whether the product is contraindicated (not recommended) for pregnant individuals, nor does it provide any guidance on dosage adjustments or special precautions for use during pregnancy.

If you are pregnant or planning to become pregnant, it’s always best to consult with your healthcare provider before using any medication or product to ensure it’s safe for you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding nursing mothers or lactation in the information provided. This means that, based on the available data, there are no known risks associated with breastfeeding while using this medication. However, it's always a good idea to consult with your healthcare provider about any concerns you may have regarding your health and breastfeeding.

Pediatric Use

This medication is intended for external use only, so it's important to keep it out of reach of children to prevent accidental ingestion or misuse. If you are using this product for yourself or for children aged 12 years and older, you can apply it to the affected area up to 3 to 4 times a day. Always ensure that you follow these guidelines to keep your child safe and to use the medication effectively.

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. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can provide the best care tailored to your needs.

Always feel free to ask questions and share all the medications and supplements you are using. This helps your provider monitor your health effectively and make informed decisions about your treatment.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place with the lid closed tightly. This helps protect it from moisture and temperature fluctuations that could affect its effectiveness.

When handling the product, always make sure to keep the storage area clean and organized to avoid contamination. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged 12 years or older. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling information.

FAQ

What is Barox S?

Barox S is an anti-inflammatory pain relieving and topical analgesic ointment intended to relieve muscle and joint pain.

What conditions does Barox S help with?

Barox S is used to relieve muscle and joint pain associated with arthritis, rheumatalgia, backaches, knee pain, and shoulder pain.

How should I use Barox S?

Apply Barox S to the affected area not more than 3 to 4 times daily, as directed.

Are there any warnings for using Barox S?

Yes, Barox S is for external use only, avoid contact with eyes, and keep it out of reach of children.

Can I use Barox S on wounds or damaged skin?

No, do not use Barox S on wounds or damaged skin.

What should I do if I experience excessive skin irritation?

Stop using Barox S and ask a doctor if excessive skin irritation occurs.

How should I store Barox S?

Store Barox S in a cool, dry place with the lid closed tightly.

Is Barox S safe to use during pregnancy or while nursing?

The provided information does not mention any specific risks or recommendations regarding use during pregnancy or nursing.

Who can use Barox S?

Barox S is intended for adults and children 12 years of age and older.

What should I do if I have redness over the affected area?

Ask a doctor before using Barox S if you have redness over the affected area.

Packaging Info

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

Packaging configurations for Barox.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

This product is intended for external use only and should not be applied to wounds or damaged skin. In the event of excessive skin irritation, usage should be discontinued, and a healthcare professional should be consulted. Prior to use, individuals with redness over the affected area are advised to seek medical advice. For optimal storage, the product should be kept in a cool, dry place with the lid securely closed. For inquiries, contact jhs3840@naver.com.

Uses and Indications

Barox S is indicated for the relief of muscle and joint pain associated with various conditions, including arthritis, rheumatalgia, backaches, knee pain, and shoulder pain. This anti-inflammatory pain-relieving topical analgesic ointment is designed to provide targeted relief for patients experiencing discomfort in these areas.

There are no teratogenic or nonteratogenic effects associated with Barox S.

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. The application should not exceed 3 to 4 times daily. Care should be taken to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

Contraindications

There are no contraindications listed for the use of this product. It is important to evaluate each patient's individual circumstances and medical history when considering treatment options.

Warnings and Precautions

For external use only, this product must be applied with caution to prevent contact with the eyes. It is imperative to keep this and all medications out of the reach of children to avoid accidental ingestion or misuse.

Healthcare professionals should advise patients to seek immediate medical assistance in the event of any adverse reactions or complications. Additionally, patients should be instructed to discontinue use and consult their healthcare provider if they experience any concerning symptoms or side effects.

No specific general precautions or laboratory tests have been provided; however, practitioners should remain vigilant and monitor patients for any unusual reactions during treatment.

Side Effects

Patients should be aware that the product is intended for external use only and must avoid contact with the eyes. It is crucial to keep this and all medications out of the reach of children to prevent accidental ingestion or misuse.

As there are no specific adverse reactions or side effects detailed in the available data, healthcare providers should monitor patients for any unexpected responses during use and report these findings as necessary.

Drug Interactions

There are no specific drug interactions or laboratory test interactions identified in the available data. Therefore, no dosage adjustments or monitoring recommendations are necessary at this time.

Packaging & NDC

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

Packaging configurations for Barox.
Details

Pediatric Use

For external use only. This medication should be kept out of the reach of children.

In pediatric patients aged 12 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. Safety and efficacy in children under 12 years of age have not been established.

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

Pregnancy

Pregnant patients should be aware that no specific information regarding the use of this product during pregnancy is provided in the prescribing information. There are no statements indicating whether the product is contraindicated in pregnancy or any associated risks to the fetus. Additionally, no dosage modifications or special precautions regarding the use of this product during pregnancy are mentioned. Healthcare professionals should consider the lack of data when advising women of childbearing potential and weigh the potential benefits against any unknown risks.

Lactation

There are no specific warnings or recommendations regarding the use of this medication in nursing mothers. Additionally, there are no specific warnings or recommendations related to lactation. Healthcare professionals should consider the absence of data when advising lactating mothers on the use of this medication.

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

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 toxicology experts for guidance on specific management strategies tailored to the substance involved.

Documentation of the incident, including the amount ingested and the time of exposure, is crucial for effective treatment 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 compound in these areas.

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. It is important to emphasize the potential risks associated with accidental ingestion by young children and to encourage patients to store medications in a secure location.

Storage and Handling

The product is supplied in a container that must be stored in a cool, dry place. It is essential to ensure that the lid is closed tightly to maintain the integrity of the product. Proper storage conditions are crucial for preserving the quality and efficacy of the product.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of no more than 3 to 4 times daily for adults and children aged 12 years and older. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

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