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Pomada Dragon Pain Relieving

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Active ingredients
  • Camphor (synthetic) 40 mg/1 g
  • Menthol 100 mg/1 g
  • Methyl Salicylate 300 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 2012
Label revision date
October 17, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 40 mg/1 g
  • Menthol 100 mg/1 g
  • Methyl Salicylate 300 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 2012
Label revision date
October 17, 2025
Manufacturer
TELEVISA CONSUMER PRODUCTS USA
Registration number
M017
NDC root
55038-001
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

You may be looking for a medication that is applied to affected areas of the skin. This treatment is suitable for adults and children aged 12 years and older, and it is typically used up to three to four times a day. If the user is under 12 years old, it is important to consult a doctor before use.

While specific details about the drug's name and mechanism of action are not provided, it is essential to follow the directions carefully to ensure safe and effective use.

Uses

You can use this medication as directed for various conditions. If you are an adult or a child aged 12 years and older, you should apply it to the affected area no more than 3 to 4 times a day. If the patient is a child under 12 years old, it’s important to consult a doctor before use.

There are no reported teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects (which refers to other types of harmful effects that do not involve birth defects) associated with this medication. Always follow the guidance provided to ensure safe and effective use.

Dosage and Administration

When using this medication, it's important to know that it is distributed by Genomma Lab USA, Inc., located in Houston, Texas, and is manufactured in China. However, the information provided does not specify how you should take or apply the medication, including the route (how it enters your body), method, or frequency (how often you should use it).

For the best results, make sure to follow any additional instructions provided by your healthcare provider or on the product packaging. If you have any questions about how to use this medication, don’t hesitate to reach out to a healthcare professional for guidance.

What to Avoid

You should avoid using this product on wounds or damaged skin, and it is important not to apply it with a heating pad. If you are considering using it for a child under 12 years of age with arthritis-like conditions, please refrain from doing so.

Make sure to follow the directions carefully and do not use it in any way other than as instructed. Keep it away from your eyes, mucous membranes, and any rashes, and avoid wrapping the area tightly with a bandage.

Side Effects

If you are considering using this product, please be aware that it is for external use only. If you have a history of allergic reactions to aspirin or salicylates, it’s important to consult your doctor before using it.

You should stop using the product and contact your doctor if you notice any redness, irritation, or rash developing. Additionally, if your condition worsens or symptoms last longer than 7 days, or if symptoms improve and then return within a few days, seek medical advice. Always check with your doctor if you see redness over the area you plan to treat.

Warnings and Precautions

This product is for external use only. If you have a history of allergic reactions to aspirin or salicylates, please consult your doctor before using it. Avoid applying it to wounds or damaged skin, and do not use it with a heating pad. It is also not recommended for children under 12 years of age who have arthritis-like conditions.

If you accidentally swallow this product, seek emergency medical help or contact a Poison Control Center right away. You should stop using the product and call your doctor if you notice any redness, irritation, or rash, if your condition worsens, or if symptoms persist for more than 7 days. Additionally, if your symptoms improve and then return within a few days, it's important to 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 potential risks associated with taking any medication. If you suspect that you or someone else may have taken too much of a medication, look out for unusual symptoms or changes in behavior.

In the event of an overdose, it is crucial to seek immediate medical help. You can contact your local emergency services or go to the nearest hospital. Remember, acting quickly can make a significant difference in ensuring safety and health. Always keep medications out of reach and follow the prescribed dosage to prevent any accidental overdosage.

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

If your child is under 12 years old and has arthritis-like conditions, it's important not to use this medication. For children in this age group, you should consult a doctor before use.

For those aged 12 and older, you can apply the medication to the affected area, but be sure to limit applications to no more than 3 to 4 times a day. Always follow your healthcare provider's guidance to ensure safe and effective use.

Geriatric Use

If you are caring for an older adult with arthritis-like conditions, it's important to note that this medication should not be used on anyone under 12 years of age. Before applying the medication, you should consult a doctor if there is any redness in the area you plan to treat. For adults and children aged 12 and older, the medication can be applied to the affected area up to three to four times a day. If the person you are caring for is under 12, please seek advice from a doctor before use.

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, especially if you have concerns about your kidney health. They can provide guidance based on your individual situation.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you or how your liver health might influence the treatment.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver condition. They can help monitor your liver function and make any necessary adjustments to your treatment plan.

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 share your complete list of medications and any health conditions you have to receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20°C and 25°C (68°F and 77°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to keep it in a clean environment to avoid contamination. Always follow any specific instructions provided for use and disposal to ensure safety and effectiveness.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times daily if you are an adult or a child aged 12 years and older. If the patient is under 12 years old, consult a doctor for guidance.

If you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this medication. Always keep it out of reach of children to prevent accidental ingestion. If the medication is swallowed, seek medical help or contact a Poison Control Center right away.

FAQ

What should I do if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before use.

How should I apply this medication?

Adults and children 12 years of age and older should apply to the affected area no more than 3 to 4 times daily. For children under 12 years of age, consult a doctor.

Are there any contraindications for using this medication?

Do not use on wounds or damaged skin, with a heating pad, or on a child under 12 years of age with arthritis-like conditions.

What should I do if I experience redness or irritation?

Stop use and ask a doctor if redness is present, irritation or rash develops, conditions worsen, or symptoms persist for more than 7 days.

Is this medication safe for children?

Children under 12 years of age should ask a doctor before use.

What should I do if I accidentally swallow this medication?

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

Can I use this medication if I have an allergy to aspirin?

If you are prone to allergic reactions from aspirin or salicylates, consult a doctor before use.

What are the storage conditions for this medication?

Store between 20°C and 25°C (68°F and 77°F).

Packaging Info

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

Packaging configurations for Pomada Dragon Pain Relieving.
Details

Drug Information (PDF)

This file contains official product information for Pomada Dragon Pain Relieving, 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 drug.

Uses and Indications

This drug is indicated for topical application in adults and children aged 12 years and older for the treatment of affected areas. It should be applied no more than 3 to 4 times daily as directed. For children under 12 years of age, consultation with a healthcare professional is advised prior to use.

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

Dosage and Administration

The product is distributed by Genomma Lab USA, Inc., located in Houston, TX 77027, and is manufactured in China.

Currently, there is no specific information available regarding the route, method, or frequency of administration for this product. Healthcare professionals are advised to refer to additional resources or clinical guidelines for further details on administration practices.

Contraindications

The product is contraindicated in the following situations:

Use is not recommended on wounds or damaged skin due to the potential for irritation and delayed healing. Application with a heating pad is contraindicated as it may increase the risk of burns or skin damage. The product should not be used in children under 12 years of age with arthritis-like conditions, as safety and efficacy have not been established in this population.

Additionally, the product should not be used otherwise than as directed. Contact with eyes, mucous membranes, or rashes must be avoided to prevent adverse reactions. Tight bandaging is also contraindicated to ensure proper circulation and prevent skin irritation.

Warnings and Precautions

For external use only. Individuals with a known allergy to aspirin or salicylates should consult a healthcare professional prior to use to assess the risk of an allergic reaction.

It is imperative to avoid application on wounds or damaged skin, as this may exacerbate irritation or lead to adverse effects. The product should not be used in conjunction with a heating pad, as this may increase the risk of skin irritation or burns. Additionally, this product is contraindicated for use in children under 12 years of age who present with arthritis-like conditions.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Users are instructed to discontinue use and consult a healthcare provider if any of the following occur: the presence of redness, irritation, or rash; worsening of the condition; or if symptoms persist beyond 7 days. Furthermore, if symptoms resolve and then recur within a few days, medical advice should be sought.

Side Effects

Patients should be aware that the product is intended for external use only. An allergy alert is in place for individuals who are prone to allergic reactions from aspirin or salicylates; such patients should consult a doctor prior to use.

In clinical practice, patients are advised to stop using the product and seek medical attention if they experience redness, irritation, or rash at the application site. Additionally, if the condition worsens or symptoms persist for more than 7 days, it is recommended that patients consult a healthcare professional. Patients should also be cautious if symptoms initially resolve and then recur within a few days, as this may warrant further evaluation by a doctor.

Before using the product, patients with redness over the affected area should consult a healthcare provider to ensure safe and appropriate use.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 Pomada Dragon Pain Relieving (camphor (synthetic) , menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Pomada Dragon Pain Relieving.
Details

Pediatric Use

Pediatric patients under 12 years of age with arthritis-like conditions should not use this medication. For children in this age group, it is advised to consult a healthcare professional before use.

For adolescents aged 12 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

Elderly patients should be aware that this medication is not indicated for use in children under 12 years of age with arthritis-like conditions. It is essential for geriatric patients to consult a healthcare provider prior to use if there is any redness over the affected area, as this may indicate a need for further evaluation.

For adults, including elderly patients aged 65 and older, the recommended application frequency is to apply the medication to the affected area no more than 3 to 4 times daily. Careful monitoring for any adverse reactions or changes in the condition of the affected area is advised, particularly in this population, due to the potential for altered pharmacokinetics and increased sensitivity to treatment.

In summary, geriatric patients should adhere to the recommended guidelines and seek medical advice when necessary to ensure safe and effective use of this medication.

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure safe use during pregnancy and lactation.

Lactation

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

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 overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, increased severity of known side effects, unusual behavioral changes, or any other atypical clinical manifestations.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. It is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for specific guidance on the management of overdose cases.

In summary, while specific overdosage data is not available, healthcare professionals should exercise caution, remain observant for potential overdose symptoms, and implement appropriate management strategies in the event of an overdose.

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 available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion. It is crucial to emphasize the importance of safeguarding the medication, as children may be particularly vulnerable to its effects.

In the event that the medication is swallowed, healthcare providers should instruct patients to seek medical help or contact a Poison Control Center immediately. Prompt action is essential to ensure the safety and well-being of the patient.

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 within the temperature range of 20°C to 25°C (68°F to 77°F) to ensure its stability and efficacy. Proper storage conditions must be maintained, and the product should be kept in a suitable container to protect it from environmental factors. Special handling requirements should be observed to preserve the integrity of the product throughout its shelf life.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of up to 3 to 4 times daily for adults and children aged 12 years and older. For children under 12 years of age, it is advised to consult a doctor regarding use.

Clinicians should counsel patients to seek advice from a health professional if they are pregnant or breastfeeding. It is crucial to keep the product out of reach of children to prevent accidental ingestion. In the event of swallowing the medication, patients should seek medical assistance or contact a Poison Control Center immediately.

Drug Information (PDF)

This file contains official product information for Pomada Dragon Pain 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 Pomada Dragon Pain 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.

Learn more in our Editorial Policy

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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.