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Katinko Pain and Itch Relieving

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Active ingredients
  • Camphor (synthetic) 11 g/100 g
  • Menthol 7.6 g/100 g
  • Methyl Salicylate 13 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2010
Label revision date
December 8, 2023
Active ingredients
  • Camphor (synthetic) 11 g/100 g
  • Menthol 7.6 g/100 g
  • Methyl Salicylate 13 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2010
Label revision date
December 8, 2023
Manufacturer
Greenstone Pharmaceutical Inc.
Registration number
M017
NDC root
52241-100

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Drug Overview

This medication is designed to provide temporary relief from minor aches and pains in muscles and joints. You might use it for conditions such as simple backache, arthritis, rheumatism, muscle strain, sprains, and bruises. Additionally, it can help alleviate pain and itching caused by insect bites and minor skin irritations.

Uses

You can use this medication for temporary relief from minor aches and pains in your muscles and joints. It can help with conditions like simple backache, arthritis, rheumatism, muscle strains, sprains, and bruises.

Additionally, if you're dealing with pain and itching from insect bites or minor skin irritations, this medication can provide relief as well. It's designed to help you feel more comfortable during those times when you need it most.

Dosage and Administration

When using this medication, you should apply it directly to the affected areas of your skin. For adults and children aged 2 years and older, you can use it up to 3 to 4 times a day. If you have a child under 2 years old, it's important to consult a doctor before using this product to ensure it's safe for them.

Make sure to follow these guidelines closely to get the best results from your treatment. Remember, applying the medication more than 3 to 4 times a day is not recommended, as this could lead to unwanted side effects.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should not bandage tightly or apply it to wounds or damaged skin, as this can lead to complications. Additionally, avoid using it on your eyes or mucous membranes, and do not combine it with a heating pad or any external heat sources, as this may increase the risk of adverse effects. Following these guidelines will help ensure your safety while using the product.

Side Effects

This product may cause allergic reactions in some people, so it's a good idea to test it on a small area of your skin before using it more widely. If you notice any skin redness or excessive irritation, or if your condition worsens, stop using the product and consult a doctor. Additionally, if your symptoms last more than 7 days or come back shortly after improving, seek medical advice. Remember, this product is for external use only, and avoid wrapping the area tightly.

Warnings and Precautions

This product is for external use only, so please avoid swallowing it. Use it exactly as directed, and do not apply it to wounds or damaged skin. It's important not to use it on your eyes or mucous membranes, and avoid using it with a heating pad or applying any external heat.

If you experience skin redness or excessive irritation, or if your condition worsens, stop using the product and contact your doctor. Additionally, if your symptoms persist for more than 7 days or return after clearing up, seek medical advice. Remember, do not bandage the area tightly. If the product is swallowed, seek emergency medical help or contact poison control immediately.

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, contact your local emergency services or go to the nearest hospital. It's always better to be safe and get checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this product during pregnancy has not been established. You should consult your healthcare provider before using it, as there may be potential risks to your fetus that are not clearly defined.

It's advised to use this product only if it is clearly needed and after discussing it with your doctor. There are no specific dosage modifications provided for pregnant individuals, so seeking guidance from a healthcare professional is essential to ensure your safety and that of 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 baby are not clearly defined.

As a precaution, you may want to consult with your healthcare provider to discuss any potential risks and to ensure that you are making the best choices for both you and your baby while breastfeeding.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 2 years and older, you can apply it to the affected areas no more than 3 to 4 times a day. However, if your child is under 2 years old, you should consult a doctor before using the medication to ensure it's safe and appropriate for them. Always prioritize your child's health and seek professional advice when needed.

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. If you or a loved one is an older adult, it’s wise to discuss any potential risks or benefits with your healthcare provider. They can help determine the best course of action based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so regular check-ins with your doctor can ensure safety and effectiveness.

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 (issues with liver function).

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. 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 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, 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 can apply this product to the affected areas of your skin 3 to 4 times a day if you are an adult or a child aged 2 years and older. If your child is under 2 years old, it's important to consult a doctor before using it.

Be aware that this product may cause an allergic reaction in some people. To ensure safety, it's a good idea to test it on a small area of skin before applying it more broadly.

FAQ

What is the drug indicated for?

The drug is indicated for temporary relief of minor aches and pains of muscles and joints, including conditions like simple backache, arthritis, rheumatism, muscle strain, sprains, and bruises.

Can this drug be used for skin irritations?

Yes, it is also indicated for temporary relief of pain and itching associated with insect bites and minor skin irritation.

What is the recommended dosage for adults and children over 2 years?

Adults and children 2 years and up should apply the drug to affected areas not more than 3 to 4 times daily.

What should I do if I am under 2 years old?

If you are under 2 years old, consult a doctor before use.

Are there any contraindications for using this drug?

No specific contraindications are mentioned, but consult a healthcare provider if pregnant or planning to become pregnant.

What precautions should I take when using this drug?

Use only as directed, do not apply to wounds or damaged skin, and avoid contact with eyes and mucous membranes.

What should I do if I experience skin irritation?

Stop use and ask a doctor if skin redness or excessive irritation occurs, or if the condition worsens.

Is this drug safe to use during pregnancy?

The safety of this product during pregnancy has not been established; caution is advised.

How should I store this drug?

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

What should I do in case of accidental ingestion?

If swallowed, get medical help or contact a poison control center immediately.

Packaging Info

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

Packaging configurations for Katinko Pain and Itch Relieving.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

SPL code 34089-3 identifies a product available in the form of 10g stickers, packaged in a box containing 10g. The product is designed for professional use, ensuring precise application and dosage.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of muscles and joints associated with conditions such as simple backache, arthritis, rheumatism, muscle strain, sprains, and bruises. Additionally, it is indicated for the temporary relief of pain and itching associated with insect bites and minor skin irritation.

There are no teratogenic or nonteratogenic effects reported for this drug.

Dosage and Administration

Adults and children aged 2 years and older should apply the medication to the affected areas no more than 3 to 4 times daily. For children under 2 years of age, it is essential to consult a healthcare professional prior to use.

The medication is to be applied topically to the affected areas, adhering to the specified frequency of administration. Care should be taken to ensure that the application does not exceed the recommended maximum of 3 to 4 times per day for the appropriate age group.

Contraindications

The product is contraindicated in the following situations:

  • Application to wounds or damaged skin is prohibited due to the risk of irritation and impaired healing.

  • Use on the eyes or mucous membranes is contraindicated to prevent potential adverse effects.

  • Tight bandaging is not recommended as it may lead to compromised circulation.

  • The application of external heat, including heating pads, is contraindicated as it may enhance absorption and increase the risk of adverse reactions.

Warnings and Precautions

For external use only. This product should be utilized strictly as directed to ensure safety and efficacy. It is imperative that the product is not applied to wounds or damaged skin, nor should it be used in or around the eyes or mucous membranes. The application of external heat, such as with a heating pad, is contraindicated.

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 if any of the following occur: skin redness or excessive irritation, worsening of the condition, persistence of symptoms beyond 7 days, or if symptoms resolve and then recur within a few days. Additionally, it is important to avoid tight bandaging of the affected area.

Side Effects

Patients may experience allergic reactions to this product, which can occur in some individuals. It is recommended to test the product on a small area of skin prior to full application to assess for any potential adverse reactions.

In addition to allergic reactions, patients should be advised to discontinue use and consult a healthcare professional if they experience skin redness or excessive irritation. Furthermore, if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days, medical advice should be sought. It is also important to note that the product is for external use only and should not be bandaged tightly.

Drug Interactions

There are no specific drug interactions reported for this medication. Additionally, no laboratory test interactions have been identified in the available data. 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 Katinko Pain and Itch Relieving (camphor (synthetic) , menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Katinko Pain and Itch Relieving.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to affected areas no more than 3 to 4 times daily. For children under 2 years of age, it is advised to consult a doctor prior to use.

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

Pregnancy

The safety of this product during pregnancy has not been established. Pregnant patients or those planning to become pregnant should consult a healthcare provider before use. Potential risks to the fetus are not clearly defined; therefore, caution is advised. There are no specific dosage modifications for pregnant individuals; however, it is essential to consult a doctor for guidance. This product should only be used if clearly needed and after a thorough discussion with a healthcare professional.

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 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 initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of specific antidotes or treatments should be considered based on the substance involved and the clinical presentation. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

Documentation of the incident, including the substance, amount ingested, and 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

Postmarketing experience has indicated that this product may provoke allergic reactions in some individuals. It is recommended that users conduct a patch test on a small area of skin prior to full application to assess for any potential sensitivity.

Patient Counseling

Healthcare providers should advise patients to seek medical help or contact a poison control center immediately if the product is swallowed. It is important to instruct patients to stop using the product and consult a doctor if they experience skin redness or excessive irritation, if their condition worsens, or if symptoms persist for more than 7 days or clear up only to recur within a few days.

Patients should be informed not to bandage the area tightly while using the product. When discussing the application of the product, healthcare providers should emphasize the importance of using it only as directed. Patients should be cautioned against applying the product to wounds or damaged skin, and they should be advised not to use it on the eyes or mucous membranes. Additionally, it is crucial to inform patients not to use the product in conjunction with a heating pad or apply external heat during use.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which are essential for identification and inventory management. It is recommended to store the product at room temperature to maintain its efficacy.

To ensure optimal preservation, the product must be protected from light exposure. Additionally, it is crucial to keep the container tightly closed when not in use to prevent contamination and degradation. Once opened, the product should be discarded after use to ensure safety and effectiveness.

Additional Clinical Information

Patients aged 2 years and older are advised to apply the product to affected areas no more than 3 to 4 times daily. For children under 2 years, consultation with a doctor is recommended prior to use. Clinicians should inform patients that the product may provoke allergic reactions in some individuals; therefore, it is advisable to conduct a patch test on a small area of skin before full application.

Drug Information (PDF)

This file contains official product information for Katinko Pain and Itch 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 Katinko Pain and Itch 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.

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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.