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Extreme Emu

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Active ingredients
  • Menthol 2.24 g/112 g
  • Methyl Salicylate 11.2 g/112 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
November 14, 2025
Active ingredients
  • Menthol 2.24 g/112 g
  • Methyl Salicylate 11.2 g/112 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
November 14, 2025
Manufacturer
Renu Laboratories, LLC
Registration number
M017
NDC root
76348-495

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Drug Overview

EXTREME EMU is a dual active botanical analgesic that contains emu oil, which is derived from the fat of the emu bird. This product is designed to temporarily relieve minor aches and pains associated with muscle and joint issues, including conditions like arthritis, simple backaches, sprains, strains, and bruises.

By using EXTREME EMU, you can find support for discomfort in your muscles and joints, helping you to feel more comfortable in your daily activities.

Uses

If you're dealing with minor aches and pains in your muscles and joints, this medication can help provide temporary relief. It's effective for discomfort caused by various conditions, including arthritis, simple backaches, sprains, strains, and bruises.

Whether you're recovering from an injury or managing chronic pain, this medication can support you in feeling more comfortable and getting back to your daily activities. Always remember to follow the recommended guidelines for use.

Dosage and Administration

You should apply the medication directly to the affected area of your skin. For both adults and children aged 12 years and older, it’s important to use the medication no more than 3 to 4 times each day. This means you can apply it several times throughout the day, but be sure to stay within that limit to ensure safe and effective use.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should not apply it to wounds or damaged skin, and avoid bandaging tightly after application. Additionally, keep the product away from your eyes; if it accidentally gets into your eyes, rinse them thoroughly with water. Lastly, do not use this product in conjunction with an electric heating pad, as this could lead to complications. Following these guidelines will help ensure your safety while using the product.

Side Effects

It's important to use this product only on the outside of your body. If you notice that your condition is getting worse, if your symptoms last longer than 7 days, or if they improve and then come back within a few days, you should stop using the product and consult your doctor. Additionally, if you develop a rash or any irritation, it's best to seek medical advice.

Warnings and Precautions

This product is intended for external use only. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately.

You should stop using this product and consult your doctor if your condition worsens, if your symptoms last longer than 7 days, or if they improve and then return within a few days. Additionally, if you notice any rash or irritation, it's important to stop use and reach out to your healthcare provider.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include unusual drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, contact your local poison control center or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

When using this medication for children, it's important to note that it is intended for adults and children aged 12 years and older. You should apply it directly to the affected area no more than 3 to 4 times a day. Always keep the medication out of reach of younger children to prevent accidental ingestion. If your child swallows any of the medication, seek medical help or contact a Poison Control Center immediately.

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 there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

It's always best to discuss your individual situation with your healthcare provider, who can offer personalized advice and ensure that any medications you take are safe and effective for you.

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 or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can avoid any potential issues and receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important to keep the tube tightly closed when not in use to maintain its integrity. If you open the tube and do not use the contents within a specified time frame, please discard it to ensure safety and effectiveness. Following these guidelines will help you handle the product safely and effectively.

Additional Information

You should apply the medication directly to the affected area, making sure to do so 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 EXTREME EMU?

EXTREME EMU is a dual active botanical analgesic that contains emu oil, designed to temporarily relieve minor aches and pains.

What conditions does EXTREME EMU help relieve?

It temporarily relieves minor aches and pains of muscles and joints due to arthritis, simple backache, sprains, strains, and bruises.

How should I use EXTREME EMU?

Apply EXTREME EMU directly to the affected area no more than 3 to 4 times daily.

Are there any precautions I should take when using EXTREME EMU?

Yes, do not apply it to wounds or damaged skin, do not bandage tightly, and avoid contact with eyes.

What should I do if I experience worsening conditions or irritation?

Stop using EXTREME EMU and ask a doctor if conditions worsen, symptoms last more than 7 days, or if a rash or irritation develops.

Is EXTREME EMU safe for children?

EXTREME EMU can be used by adults and children 12 years of age and older.

What should I do if EXTREME EMU is swallowed?

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

Can I use EXTREME EMU if I am pregnant or breastfeeding?

You should ask a health professional before using EXTREME EMU if you are pregnant or breastfeeding.

How should I store EXTREME EMU?

Store EXTREME EMU at room temperature, protect it from light, and keep the tube tightly closed when not in use.

Packaging Info

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

Packaging configurations for Extreme Emu.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscle and joint conditions, including arthritis, simple backache, sprains, strains, and bruises.

Limitations of Use: This medication is intended for short-term use and should not be used as a substitute for more comprehensive treatment of underlying conditions.

Dosage and Administration

Adults and children 12 years of age and older should apply the medication directly to the affected area. The application should not exceed 3 to 4 times daily. Care should be taken to ensure that the medication is applied only to the areas requiring treatment.

Contraindications

The product is contraindicated in the following situations:

Application to wounds or damaged skin is prohibited due to the potential for irritation or adverse reactions. Tight bandaging is not recommended as it may impede circulation and exacerbate skin irritation. The product should not be used in or near the eyes; in the event of contact, thorough rinsing with water is necessary to prevent ocular irritation. Additionally, the use of an electric heating pad in conjunction with this product is contraindicated, as it may increase the risk of skin burns or other complications.

Warnings and Precautions

For external use only. In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Healthcare professionals are advised to instruct patients to discontinue use and consult a physician if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or symptoms resolve and then recur within a few days. Additionally, if a rash or irritation develops, patients should be advised to stop use and seek medical advice.

Side Effects

For external use only. Patients should discontinue use and consult a healthcare professional if conditions worsen, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Additionally, if a rash or irritation develops, it is advised to stop use and seek medical advice.

Drug Interactions

There are currently no documented drug interactions associated with the use of this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

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

Packaging configurations for Extreme Emu.
Details

Pediatric Use

Pediatric patients aged 12 years and older may apply the medication directly to the affected area no more than 3 to 4 times daily. It is important to keep the product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

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 therapeutic response, given the lack of targeted data for this population.

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional before using this medication. The safety of this drug during pregnancy has not been established, and potential risks to fetal outcomes are not fully known. Therefore, it is essential for women of childbearing potential to seek medical advice prior to use to ensure appropriate management and consideration of any potential risks.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data regarding the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating mothers.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the lack of information necessitates careful clinical judgment and monitoring.

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

There is currently no specific information available regarding overdosage for this medication. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Continuous monitoring of vital signs and clinical status is essential. If symptoms of overdosage are observed, appropriate interventions should be implemented based on the patient's condition.

Healthcare professionals should also consider contacting a poison control center or a medical toxicologist for guidance on management strategies tailored to the specific situation.

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 elucidate these aspects of nonclinical toxicology.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be instructed 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. Additionally, patients should be informed to stop using the product and seek medical advice if they experience any rash or irritation.

While using this product, patients must be cautioned against applying it to wounds or damaged skin. They should also be advised not to bandage the area tightly after application. It is important to inform patients that the product should not be used in or near the eyes; if contact occurs, they should rinse their eyes thoroughly with water. Furthermore, patients should be warned against using the product in conjunction with an electric heating pad.

Storage and Handling

The product is supplied in a tube format, with specific handling and storage requirements to ensure its integrity and efficacy. It should be stored at room temperature, away from direct light exposure. To maintain the product's quality, it is essential to keep the tube tightly closed when not in use. Additionally, any unused product should be discarded after opening if it is not utilized within a specified time frame.

Additional Clinical Information

Patients aged 12 years and older are advised to apply the medication directly to the affected area no more than 3 to 4 times daily. 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 Extreme Emu, 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 Extreme Emu, 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.