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Katinko External Analgesic Oil

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Active ingredients
  • Camphor (synthetic) 50 mg/1 mL
  • Menthol 160 mg/1 mL
  • Methyl Salicylate 300 mg/1 mL
Other brand names
Dosage form
Oil
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2023
Label revision date
December 8, 2023
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 50 mg/1 mL
  • Menthol 160 mg/1 mL
  • Methyl Salicylate 300 mg/1 mL
Other brand names
Dosage form
Oil
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 2023
Label revision date
December 8, 2023
Manufacturer
Greenstone Pharmaceutical Inc.
Registration number
M017
NDC root
52241-301
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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 provide temporary relief from minor aches and pains in your muscles and joints. It can be helpful if you're experiencing discomfort due to everyday activities or minor injuries. While the specific details about how it works are not provided, its primary purpose is to alleviate those bothersome aches, allowing you to feel more comfortable in your daily life.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It’s designed to help you feel more comfortable when dealing with these everyday discomforts.

Rest assured, there are no known teratogenic effects (which means it doesn’t cause birth defects) associated with this medication, making it a safer option for those who may be concerned about such risks.

Dosage and Administration

If you are an adult or a child aged 3 years and older, you can apply the medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results.

For children under 3 years of age, it’s important to consult a doctor before using this medication. This will help ensure that it is safe and appropriate for their specific needs. Always follow your healthcare provider's advice for the best care.

What to Avoid

It's important to use this medication safely to ensure your well-being. You should never apply it to wounds or damaged skin, as this can lead to complications. Additionally, avoid bandaging the area tightly, as this may cause irritation or other issues. Always follow the directions provided and do not use the medication in any way that is not specified. By adhering to these guidelines, you can help ensure that you use the medication effectively and safely.

Side Effects

When using this product, it's important to apply it only to the skin and avoid contact with your eyes or any mucous membranes. Do not use it on wounds or damaged skin, and avoid wrapping the area tightly. If your condition worsens, symptoms last more than 7 days, or if irritation becomes excessive, stop using the product and consult a doctor.

Keep this product out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately to prevent accidental poisoning.

Warnings and Precautions

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

If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult your doctor. Additionally, if you experience excessive skin irritation, it's important to seek medical advice.

In case of accidental swallowing, seek emergency medical help immediately or contact a Poison Control Center to prevent poisoning.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, it’s important to act quickly. Contact a medical professional or call a Poison Control Center immediately to prevent accidental poisoning.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. Always err on the side of caution and seek help if you notice anything concerning. Remember, timely action can make a significant difference in ensuring safety and health.

Pregnancy Use

You can use Katinko External Analgesic Oil during pregnancy, as there are no specific warnings or precautions mentioned regarding its use. The information available does not indicate that the product is contraindicated (not recommended) for pregnant individuals, nor does it suggest any risks to the fetus. Additionally, there are no dosage modifications or special precautions required for those who are pregnant.

As always, it's a good idea to consult with your healthcare provider before using any new product during pregnancy to ensure it’s safe for you and your baby.

Lactation Use

If you are breastfeeding, you can use Katinko External Analgesic Oil without specific warnings or recommendations against it. Currently, there is no information suggesting that this product is passed into breast milk or poses any risk to your nursing infant. Always feel free to consult with your healthcare provider if you have any concerns about using new products while breastfeeding.

Pediatric Use

If your child is under 3 years old, it's important to consult a doctor before using this medication. For children aged 3 years and older, you can apply the medication to the affected area, but be sure to do this no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

When it comes to using Katinko External Analgesic Oil, there is no specific information available about how it should be used by older adults. This means that there are no special dosage adjustments, safety concerns, or precautions outlined for elderly patients.

If you are an older adult or a caregiver, it's always a good idea to consult with a healthcare professional before starting any new medication or treatment. They can provide personalized advice based on individual health needs and conditions.

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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

Drug Interactions

It's great to know that there are no reported interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective.

Always keep your healthcare provider informed about any changes in your health or new medications you may start. Open communication helps prevent any potential issues and supports your overall well-being.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature and keep it away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination. Once you open the container, please remember to discard it after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply the medication topically to the affected area, using it no more than 3 to 4 times a day. This means you can put it directly on the skin where you need relief, but be careful not to exceed the recommended frequency. If you have any questions about how to use the medication or its effects, consult your healthcare provider for guidance.

FAQ

What is the primary use of this drug?

This drug is used for the temporary relief of minor aches and pains of muscles and joints.

How should I apply this drug?

For adults and children 3 years of age and older, apply to the affected area not more than 3 to 4 times daily. Children under 3 years of age should consult a doctor.

Are there any warnings I should be aware of?

Yes, this product is for external use only. Avoid contact with eyes or mucous membranes, and do not apply to wounds or damaged skin.

What should I do if my condition worsens?

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

What should I do if the product is swallowed?

If swallowed, get medical help or contact a Poison Control Center right away to avoid accidental poisoning.

Is this drug safe to use during pregnancy?

There are no specific warnings or contraindications regarding the use of this drug during pregnancy mentioned in the provided text.

Can nursing mothers use this drug?

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

How should I store this drug?

Store at room temperature, protect from light, and keep the container tightly closed. Discard after opening.

Packaging Info

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

Packaging configurations for Katinko External Analgesic Oil.
Details

Drug Information (PDF)

This file contains official product information for Katinko External Analgesic Oil, 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 specific description details are provided in the text.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles and joints.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

For adults and children aged 3 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. It is important to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

For children under 3 years of age, it is advised to consult a healthcare professional prior to use to determine the appropriate course of action.

Contraindications

The product should not be applied to wounds or damaged skin due to the potential for irritation or adverse reactions. Additionally, it is contraindicated to bandage tightly, as this may impede circulation. Use of the product should strictly adhere to the provided directions; any deviation from these instructions is not recommended.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes or mucous membranes. The product should not be applied to wounds or damaged skin, and it is essential to refrain from tightly bandaging the area of application. Use of this product should strictly adhere to the directions provided; any deviation from these instructions is not recommended.

Healthcare professionals should advise patients to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Additionally, if excessive irritation of the skin develops, medical consultation is warranted.

In cases of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted to prevent potential poisoning.

Side Effects

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

In clinical practice, patients are instructed to discontinue use and consult a healthcare professional if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Furthermore, if excessive irritation of the skin develops, medical advice should be sought.

It is important to keep this product out of the reach of children. In the event of accidental ingestion, patients should seek medical help or contact a Poison Control Center immediately to prevent potential poisoning.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Katinko External Analgesic Oil.
Details

Pediatric Use

Pediatric patients under 3 years of age should consult a doctor prior to use. For children aged 3 years and older, the recommended application is to the affected area not more than 3 to 4 times daily.

Geriatric Use

There is no specific information regarding the use of Katinko External Analgesic Oil in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when considering the use of this product in elderly patients, as individual responses may vary. Monitoring for any adverse effects or unusual reactions is advisable when administering this product to the geriatric population.

Pregnancy

The use of Katinko External Analgesic Oil during pregnancy has not been specifically addressed in the available prescribing information. There are no warnings or precautions regarding its use in pregnant patients, nor does the insert indicate any contraindications or potential risks to the fetus. Additionally, no dosage modifications or special precautions for individuals who are pregnant have been provided. Healthcare professionals should consider the absence of data when advising pregnant patients and weigh the benefits against any potential risks.

Lactation

There are no specific warnings or recommendations regarding the use of Katinko External Analgesic Oil in lactating mothers. Additionally, there are no statements concerning the potential for excretion of the product in breast milk or any associated risks to 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 event of an overdosage, immediate medical intervention is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical assistance or contact a Poison Control Center without delay. This prompt action is essential to mitigate the risk of accidental poisoning and to ensure appropriate management of the situation.

Healthcare providers should be prepared to assess the patient for potential symptoms associated with overdosage, which may vary depending on the specific substance involved. Monitoring and supportive care may be necessary, and treatment should be tailored to the individual case based on clinical presentation and the substance ingested.

In summary, swift action and professional guidance are paramount in managing overdosage cases to prevent serious health consequences.

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 question. Further studies may be necessary to fully evaluate the nonclinical toxicology profile.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Patients should be advised to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed, as this may lead to accidental poisoning.

Healthcare providers should instruct patients to discontinue use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, patients should be informed to stop using the product if they experience excessive irritation of the skin.

While using this product, patients must be cautioned to avoid contact with the eyes and mucous membranes. They should not apply the product to wounds or damaged skin, and it is important to avoid tight bandaging of the area. Patients should only use the product as directed and not for any other purposes.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with application to the affected area recommended no more than 3 to 4 times daily. 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 Katinko External Analgesic Oil, 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 Katinko External Analgesic Oil, 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.