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Balm Stick

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This product has been discontinued

Active ingredients
  • Camphor (synthetic) 12 g/100 g
  • Menthol 13 g/100 g
  • Methyl Salicylate 7 g/100 g
Other brand names
Dosage form
Stick
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2016
Label revision date
December 27, 2021
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 12 g/100 g
  • Menthol 13 g/100 g
  • Methyl Salicylate 7 g/100 g
Other brand names
Dosage form
Stick
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 2016
Label revision date
December 27, 2021
Manufacturer
Indo Abadi Sari Makmur, PT
Registration number
part348
NDC root
70815-001
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

This medication is designed to relieve various types of discomfort, including muscle pains, lumbago (lower back pain), insect bites, and itching. It works by targeting the source of your pain and discomfort, helping to provide you with relief when you need it most.

If you're experiencing any of these issues, this medication may be a helpful option to consider for easing your symptoms and improving your comfort. Always consult with a healthcare professional for personalized advice and to ensure it's the right choice for you.

Uses

You can use this medication to help relieve various types of discomfort. It is effective for easing muscle pains, which can be caused by strain or overuse. If you're dealing with lumbago (lower back pain), this medication may also provide you with some relief. Additionally, it can help soothe the irritation from insect bites and alleviate itching, making it a versatile option for managing these common issues.

Dosage and Administration

You should apply the medication directly to the affected area whenever you feel it's necessary. This means you can use it as often as you need to help manage your symptoms. Just make sure to follow any specific instructions provided by your healthcare provider to ensure you're using it safely and effectively.

What to Avoid

It's important to be aware of certain situations where you should stop using this product and consult your doctor. If your condition worsens, if symptoms last longer than 7 days, or if symptoms improve and then return within a few days, you should seek medical advice. Additionally, if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, stop using the product immediately.

For those using this product for arthritis pain, you should also consult your doctor if the pain persists for more than 10 days, if you notice any redness, or if the product is being used for children under 12 years of age. Always prioritize your health and safety by following these guidelines.

Side Effects

You should be aware of some potential side effects when using this medication. If you notice that 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 your doctor. Additionally, if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, seek medical advice.

For those using this medication for arthritis pain, you should also stop use and contact your doctor if the pain persists for more than 10 days, if you notice any redness, or if the condition affects a child under 12 years of age. Remember, this product is for external use only and should not be applied directly into the nostrils or used on children under 2 years old.

Warnings and Precautions

This product is for external use only and should not be used on children under 2 years old. Please avoid applying it directly into the nostrils, and always keep it out of reach of children.

You should stop using this product and contact 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, or a skin rash. If you are using it for arthritis pain, stop use and consult your doctor if the pain lasts more than 10 days, if you notice redness, or if the condition affects a child aged 12 years or younger.

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, or if you are unsure, 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 health and safety.

Pregnancy Use

While the information provided does not specify any particular safety concerns or dosage modifications for pregnant individuals, it is always important to approach any medication with caution during pregnancy. Since there are no special precautions mentioned regarding use during this time, you should consult with your healthcare provider before taking any medication. They can help you understand the potential risks and benefits based on your specific situation. Always prioritize open communication with your doctor to ensure the best outcomes for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the use of this medication during nursing. This means that the effects on breast milk and your nursing infant are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding. They can help you weigh the potential risks and benefits to ensure the safety of both you and your baby.

Pediatric Use

It's important to be cautious when considering this medication for children. You should not use it for children under 2 years of age. For children aged 12 and older, if your child has pain that lasts more than 10 days or shows signs of redness, it's essential to consult a healthcare professional before continuing treatment. Always prioritize your child's safety and well-being by following these guidelines.

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 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 detailed guidelines available regarding how the medication may affect you or how your liver health might influence the medication's effectiveness or safety.

Given this lack of information, it's crucial to discuss your liver condition with your healthcare provider before starting any new medication. They can help determine the best approach for your treatment and ensure that your liver health is taken into account.

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 monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This way, you can work together to ensure your treatment is safe and effective.

Storage and Handling

To ensure the safety and effectiveness of your product, always keep the container tightly closed when not in use. This helps prevent contamination and maintains the integrity of the contents. Store the product in a cool, dry place at a temperature between 16 to 30 degrees Celsius (69 to 86 degrees Fahrenheit).

By following these simple storage guidelines, you can help ensure that the product remains safe and effective for your use. If you have any questions about handling or disposal, please refer to the specific instructions provided with your product.

Additional Information

The medication is applied topically, meaning you will use it directly on the skin. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences. If you have any specific questions or concerns about using this medication, it's best to consult your healthcare provider for personalized advice.

FAQ

What is the general use of this drug?

This drug relieves muscle pains, lumbago, insect bites, and itching.

How should I apply this drug?

Apply to the affected area as needed.

Are there any contraindications for this drug?

No specific contraindications are mentioned.

What should I do if my condition worsens?

Stop use and ask your doctor if your condition worsens or if symptoms persist for more than 7 days.

Is this drug safe for children?

Do not use this drug for children below 2 years of age.

What should I do if I experience excessive skin irritation?

Stop use and consult your doctor if excessive irritation of the skin develops.

Can I use this drug during pregnancy?

There is no specific information regarding the use of this drug during pregnancy.

What are the storage conditions for this drug?

Store the drug at 16 to 30 degrees centigrade (69 to 86 Fahrenheit) and keep the container tightly closed.

What should I do if I experience nausea or abdominal discomfort?

Stop use and ask your doctor if you experience nausea, vomiting, abdominal discomfort, diarrhea, or skin rash.

Is there any information about drug interactions?

No specific drug interactions are mentioned.

Packaging Info

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

Packaging configurations for Balm Stick.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available data.

Uses and Indications

This drug is indicated for the relief of muscle pains, lumbago, insect bites, and itching.

There are no teratogenic or nonteratogenic effects mentioned in the available data.

Dosage and Administration

The medication should be applied to the affected area as needed. Healthcare professionals are advised to assess the specific condition and severity of the patient's symptoms to determine the appropriate frequency and amount of application. It is important to ensure that the area is clean and dry prior to application to maximize the efficacy of the treatment.

Contraindications

There are no specified contraindications for this product. However, healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: worsening of the condition, persistence of symptoms beyond 7 days, recurrence of symptoms after initial resolution within a few days, development of excessive skin irritation, or the onset of nausea, vomiting, abdominal discomfort, diarrhea, or skin rash. Additionally, for patients using the product for arthritis-related pain, it is recommended to seek medical advice if pain persists for more than 10 days, if redness is present, or if the patient is a child under 12 years of age.

Warnings and Precautions

External use only is mandated for this product. It is contraindicated for use in children under 2 years of age, and direct application into the nostrils should be strictly avoided.

To ensure safety, this product must be kept out of reach of children. Healthcare professionals should advise patients to discontinue use and consult a physician 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.

  • There is excessive irritation of the skin.

  • Symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash develop.

In cases where the product is used for arthritis-related pain, patients should seek medical advice if pain persists for more than 10 days, if redness is observed, or if the product is being used in children aged 12 years or younger. Regular monitoring of these parameters is essential to ensure patient safety and effective management of symptoms.

Side Effects

Patients using this product may experience a range of adverse reactions. Serious adverse reactions include excessive irritation of the skin, nausea, vomiting, abdominal discomfort, diarrhea, or skin rash. In clinical settings, participants are advised to stop use and consult a healthcare professional if any of these symptoms occur.

Common adverse reactions may also warrant attention. Patients should discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve only to recur within a few days. Additionally, when using this product for arthritis-related pain, patients should be cautious if pain persists for more than 10 days, if redness is present, or if the product is being used in children aged 12 years or younger.

It is important to note that this product is for external use only and should not be applied directly into the nostrils. Furthermore, it is contraindicated for use in children under 2 years of age.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Balm Stick.
Details

Pediatric Use

Pediatric patients under 2 years of age should not be administered this medication. For children aged 12 years and older, it is important to monitor for specific conditions; if pain persists for more than 10 days or if redness is present, further evaluation is warranted.

Geriatric Use

There is no specific information available 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.

Pregnancy

Pregnant patients should be aware that there are no specific safety concerns detailed regarding the use of this medication during pregnancy. Additionally, there are no dosage modifications recommended for pregnant individuals. Current data does not indicate any special precautions that need to be taken when administering this medication to pregnant patients. As always, healthcare professionals should weigh the potential benefits against any risks when considering treatment options for women of childbearing potential.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or any lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. Further research may be necessary to fully understand the implications for breastfed infants.

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, as the clinical presentation can vary depending on the substance involved and the individual patient's response. Common symptoms of overdose may include, but are not limited to, altered mental status, cardiovascular instability, and respiratory distress.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs. The use of activated charcoal may be considered if the patient presents within a suitable timeframe and is deemed appropriate based on clinical judgment.

Further management should be guided by the specific circumstances of the overdose, including the substance involved and the patient's clinical status. Consultation with a poison control center or toxicology expert is recommended for tailored guidance and intervention strategies.

Documentation of the incident, including the substance, amount ingested, time of ingestion, and any symptoms observed, is crucial for ongoing management and treatment decisions.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. Patients should be instructed to discontinue use and consult a healthcare professional 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, when using the medication for arthritis-related pain, patients should be informed to seek medical advice if the pain persists for more than 10 days, if redness is present, or if the medication is being used in children under 12 years of age. It is essential for healthcare providers to ensure that patients understand these critical points to promote safe and effective use of the medication.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain integrity. It should be stored at a temperature range of 16 to 30 degrees Celsius (69 to 86 degrees Fahrenheit) to ensure optimal stability and efficacy. Proper handling and storage conditions are essential for preserving the quality of the product.

Additional Clinical Information

The route of administration for the product is topical. There are no additional details available regarding laboratory tests, abuse information, patient counseling information, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Balm Stick, 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 Balm Stick, 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.