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Neotica

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This product has been discontinued

Active ingredients
  • Menthol 56.4 mg/1 g
  • Methyl Salicylate 125 mg/1 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 2018
Label revision date
October 25, 2022
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol 56.4 mg/1 g
  • Methyl Salicylate 125 mg/1 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 2018
Label revision date
October 25, 2022
Manufacturer
Lost Tree Health, LLC
Registration number
part348
NDC root
72398-000
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (3 NDCs)
Packaging & NDC Codes (3)

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

Neotica Creme is a topical cream designed to provide temporary relief from minor aches and pains in muscles and joints. It is formulated to help soothe discomfort, making it a useful option for those experiencing muscle or joint soreness.

When applied to the affected area, Neotica Creme works to alleviate pain, allowing you to feel more comfortable and active throughout your day.

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 this 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 use. This will help ensure the safety and effectiveness of the treatment for younger children. Always follow your healthcare provider's advice regarding the use of this medication.

What to Avoid

It's important to use this medication safely. You should not apply it to wounds or any damaged skin, as this can lead to complications. Additionally, avoid bandaging the area tightly after application, as this may interfere with the medication's effectiveness and could cause irritation. Always follow these guidelines to ensure your safety and the best possible outcome from your treatment.

Side Effects

When using this product, it's important to apply it only as directed and avoid contact with your eyes and mucous membranes. Do not use it on wounds or damaged skin, and refrain from tightly bandaging the area. If your condition worsens, symptoms persist for more than 7 days, or if they clear up and then return within a few days, stop using the product and consult a doctor. Additionally, if you experience excessive skin irritation, seek medical advice.

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

Warnings and Precautions

This product is intended for external use only, so be sure to follow the directions carefully. Avoid getting it in your eyes or on sensitive areas like mucous membranes, and do not apply it to any wounds or damaged skin. It's also important not to wrap the area tightly after application.

If your condition worsens, if symptoms last more than 7 days, or if they clear up and then return within a few days, stop using the product and consult your doctor. Additionally, if you experience excessive skin irritation, seek medical advice. In case of accidental swallowing, please get medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

There is currently no specific information available about the use of this product during pregnancy. The insert does not indicate whether the product is contraindicated (not recommended) for pregnant individuals or if there are any associated risks to the developing fetus. Additionally, there are no dosage modifications or special precautions mentioned for use during pregnancy.

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

Lactation Use

If you are breastfeeding, you can use Neotica cream without specific warnings or recommendations against it. Currently, there is no information available about whether the ingredients in Neotica cream pass into breast milk or if they pose any risk to your nursing infant.

As always, if you have any concerns or questions about using this product while breastfeeding, it's a good idea to consult with your healthcare provider for personalized advice.

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 and older, you can apply the medication to the affected area, but be sure not to exceed 3 to 4 applications in a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

While there is no specific information about the use of Neotica (menthol, methyl salicylate cream) in older adults, it’s always important to approach any new treatment with caution. Since the drug insert does not mention dosage adjustments or safety concerns for elderly patients, you should consult with a healthcare professional before using this product. They can provide personalized advice based on your health needs and any other medications you may be taking.

As a caregiver or older adult, staying informed and discussing any potential risks or benefits with your doctor can help ensure safe and effective use of this cream.

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 be adjusted 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 condition. They can help monitor your kidney health and make any necessary changes 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 should be used if you have hepatic impairment (issues with liver function).

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 you understand how to manage your treatment effectively.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known interactions between this medication and other drugs or laboratory tests. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always share your complete list of medications and any lab tests you undergo to avoid any potential issues.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place where the temperature does not exceed 86°F (30°C). Keeping it within this temperature range helps maintain its effectiveness and safety.

When handling the product, always do so with clean hands and in a clean environment to avoid contamination. If you have any specific disposal instructions, please follow them carefully to ensure safe and responsible disposal.

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 3 years and older. If the patient is under 3 years old, it's important to consult a doctor before use.

FAQ

What is Neotica Creme used for?

Neotica Creme is used for the temporary relief of minor aches and pains of muscles and joints.

How should I apply Neotica Creme?

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

Are there any contraindications for using Neotica Creme?

No contraindications are listed for Neotica Creme.

What precautions should I take when using Neotica Creme?

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

What should I do if I experience excessive skin irritation?

Stop using Neotica Creme and ask a doctor if excessive irritation of the skin develops.

Is Neotica Creme safe to use during pregnancy?

There is no specific information regarding the use of Neotica Creme during pregnancy, and no contraindications are mentioned.

Can nursing mothers use Neotica Creme?

There are no specific warnings or recommendations regarding the use of Neotica Creme in nursing mothers.

What should I do if Neotica Creme is swallowed?

If swallowed, get medical help or contact a Poison Control Center right away.

What is the storage requirement for Neotica Creme?

Store Neotica Creme at temperatures not exceeding 86°F / 30°C.

Packaging Info

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

Packaging configurations for Neotica.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Neotica Creme is a topical formulation designed for application to the skin. It is packaged in a 15g tube, facilitating convenient use. The specific active ingredient is not detailed in the provided information, nor are the inactive ingredients specified.

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 and lead to further complications.

Warnings and Precautions

This product is intended for external use only. Healthcare professionals should advise patients to use the product strictly as directed to ensure safety and efficacy. It is imperative to avoid contact with the eyes and mucous membranes, as such exposure may lead to adverse effects. Additionally, the product should not be applied to wounds or damaged skin, and patients should be cautioned against applying tight bandages over the treated area to prevent complications.

Patients should be instructed 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. Furthermore, if excessive skin irritation develops, it is essential to stop use and consult a healthcare provider.

In the event of accidental ingestion, immediate medical assistance should be sought, or the patient should contact a Poison Control Center without delay. These precautions are critical to ensure the safe use of the product and to mitigate potential risks associated with its application.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is crucial to follow the directions provided and to avoid contact with the eyes and mucous membranes. The product should not be applied to wounds or damaged skin, and tight bandaging is not recommended.

In clinical practice, patients are advised 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. Additionally, if excessive irritation of the skin develops, medical advice should be sought.

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

Drug Interactions

There are no documented drug interactions associated with this medication. Additionally, there are no reported interactions between this medication and laboratory tests. Therefore, no specific dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Neotica.
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 Neotica (menthol, methyl salicylate cream) in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when administering this product to elderly patients, as the absence of data necessitates careful monitoring for any potential adverse effects or unique responses in this population. It is advisable to consider the overall health status and comorbidities of geriatric patients when determining the appropriateness of this treatment.

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 use 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 Neotica cream in lactating mothers. Additionally, there is no information available about the potential for excretion of Neotica cream 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 this medication. Consequently, there are no 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 prescribing information.

Overdosage

In the event of an overdosage, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential.

Management procedures should include supportive care and symptomatic treatment as necessary. Continuous evaluation of the patient's condition is recommended to address any complications that may arise.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available for SPL code 90375-7.

Patient Counseling

Patients should be advised to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important for healthcare providers to instruct patients to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

Patients should also be informed to stop using the product and consult a healthcare professional if they experience excessive skin irritation. It is essential to emphasize that the product should be used only as directed.

Healthcare providers should caution patients to avoid contact with the eyes and mucous membranes while using the product. Additionally, patients should be advised not to apply the product to wounds or damaged skin and to refrain from tightly bandaging the area where the product is applied.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at temperatures not exceeding 86°F (30°C) to maintain its integrity and efficacy. Proper storage conditions should be observed to ensure optimal performance and safety.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3 to 4 times daily for adults and children aged 3 years and older. For children under 3 years of age, consultation with a doctor is advised prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

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