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Shennong Analgesic Plaster

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This product has been discontinued

Active ingredients
  • Camphor (synthetic) 4.28 mg/100 mg
  • Menthol 2.84 mg/100 mg
  • Methyl Salicylate 1.4 mg/100 mg
Other brand names
Dosage form
Plaster
Route
Transdermal
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2016
Label revision date
March 16, 2016
Active ingredients
  • Camphor (synthetic) 4.28 mg/100 mg
  • Menthol 2.84 mg/100 mg
  • Methyl Salicylate 1.4 mg/100 mg
Other brand names
Dosage form
Plaster
Route
Transdermal
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2016
Label revision date
March 16, 2016
Manufacturer
Guangdong Zhanjiang Jimin Pharmaceutical Co. Ltd
Registration number
part348
NDC root
68048-922

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Drug Overview

This medication is designed to provide temporary relief from minor aches and pains in your muscles and joints. It can help alleviate discomfort caused by conditions such as simple backache, arthritis, strains, bruises, and sprains. By targeting these specific areas, it aims to make daily activities more comfortable for you.

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 various conditions, including simple backaches, arthritis, strains, bruises, and sprains.

You can rely on it to ease discomfort from these common issues, allowing you to get back to your daily activities with less pain. Remember, while it can help with these specific types of pain, it's always a good idea to consult with a healthcare professional if you have any concerns or if your symptoms persist.

Dosage and Administration

To use the plaster effectively, start by cleaning and drying the area where you plan to apply it. Once the skin is ready, carefully remove the paper backing from the plaster and place it directly on the affected area.

You should change the plaster as needed, but remember not to apply it more than 3 to 4 times a day. If you are using this plaster for a child under 12 years old, it’s important to contact a doctor for guidance before proceeding.

What to Avoid

You should avoid using this product on wounds, irritated, or damaged skin unless directed by a healthcare professional. It's important to keep this product out of reach of children to prevent accidental poisoning. If swallowed, seek medical help or contact a Poison Control Center immediately.

Additionally, be careful to avoid contact with your eyes or mucous membranes, and do not apply a tight bandage over the area where the product is used. Following these guidelines will help ensure your safety while using this product.

Side Effects

You should be aware that this product is for external use only and should not be used by pregnant women. If you notice that your condition worsens, or if your symptoms last longer than 7 days, it's important to stop using the product and consult a doctor. Additionally, if your symptoms improve and then return within a few days, or if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, seek medical advice.

If you are using this product for arthritis pain, stop use and contact a healthcare professional if your pain lasts more than 10 days or if you notice any redness. Your health and safety are important, so please pay attention to these signs.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any internal areas. If you are pregnant, do not use this product. Be careful to keep it away from your eyes and mucous membranes, and avoid wrapping the area tightly with bandages.

If your condition worsens, or if your symptoms last more than 7 days, please stop using the product and contact your doctor. You should also reach out to your doctor if your symptoms improve and then return within a few days, if you experience excessive skin irritation, or if you have nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash. For those using it for arthritis pain, stop use if the pain lasts more than 10 days or if you notice any redness.

In case of accidental swallowing, seek emergency medical help or contact a Poison Control Center 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 concerned about a possible overdose, 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 professional assistance if you think you or someone else may have taken too much of a medication.

Pregnancy Use

It is important to avoid using this medication if you are pregnant. The potential risks to your developing baby are significant, and it is best to prioritize safety during this critical time. If you are planning to become pregnant or are currently pregnant, please consult your healthcare provider for guidance and alternative options. Your health and the health of your baby are paramount, so always seek professional advice before taking any medication.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that this medication should not be used by pregnant women. While the information about its effects on breastfeeding is limited, always consult your healthcare provider for personalized advice. They can help you weigh the benefits and risks, ensuring the safety of both you and your baby.

Pediatric Use

If you have a child under 12 years old, it's important to consult with a doctor before using this medication. This ensures that your child receives the appropriate care and guidance tailored to their specific needs. Always prioritize their health and safety by seeking professional advice when it comes to medications.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider for personalized advice. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

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 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 differently due to your liver health.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have about taking this medication with your liver condition. They can help ensure that your treatment is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This way, you can work together to ensure your treatment is safe and effective.

Storage and Handling

To ensure the best performance of your product, always keep it tightly closed when not in use. Store it at room temperature, ideally between 20 to 25 °C (68-77 °F). This helps maintain its effectiveness and safety.

When handling the product, make sure to do so in a clean environment to avoid contamination. Following these simple storage and handling guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is the drug used for?

The drug is used for the temporary relief of minor aches and pains of muscles and joints due to conditions like simple backache, arthritis, strains, bruises, and sprains.

How should I apply the plaster?

Clean and dry the affected area, remove the paper backing from the plaster, and apply it to the affected area. Change plasters as needed, but do not apply more than 3 to 4 times daily.

Are there any contraindications for this drug?

Do not use the drug on wounds, irritated or damaged skin, and avoid using it otherwise than as directed.

What should I do if I accidentally swallow the drug?

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

What are the warnings associated with this drug?

This drug is for external use only and should not be used on pregnant women.

When should I stop using the drug and contact a doctor?

Stop using the drug if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation occurs.

Is this drug safe for children?

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

How should I store the drug?

Store the drug tightly closed at room temperature, between 20 to 25 °C (68-77 °F).

Packaging Info

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

Packaging configurations for Shennong Analgesic Plaster.
Details

Drug Information (PDF)

This file contains official product information for Shennong Analgesic Plaster, 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 additional 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. Specifically, it is effective for conditions such as simple backache, arthritis, strains, bruises, and sprains.

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

Dosage and Administration

The affected area should be cleaned and dried prior to application. After preparing the skin, the paper backing from the plaster must be removed. The plaster should then be applied directly to the affected area.

Plasters may be changed as needed, but it is important not to exceed 3 to 4 applications per day. For patients under 12 years of age, it is recommended to consult a physician before use.

Contraindications

Use is contraindicated in the following situations:

Application on wounds, irritated, or damaged skin is prohibited unless specifically directed.

To prevent accidental poisoning, keep out of reach of children. In the event of ingestion, seek medical assistance or contact a Poison Control Center immediately.

Avoid contact with the eyes and mucous membranes.

Tight bandaging is not recommended.

Warnings and Precautions

For external use only. This product is contraindicated in pregnant women.

General precautions should be observed to ensure safe application. It is essential to avoid contact with the eyes or mucous membranes, as this may lead to irritation. Additionally, bandaging should not be applied tightly to the treated area to prevent complications.

Patients are advised to discontinue use and consult a healthcare professional under the following circumstances: if the condition worsens; if symptoms persist for more than 7 days; if symptoms resolve and then recur within a few days; if excessive skin irritation develops; if gastrointestinal symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occur; or when using the product for arthritis pain, if pain persists for more than 10 days or if redness is present.

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

Side Effects

Patients should be aware that the product is intended for external use only and should not be used by pregnant women.

In clinical practice, it is advised that patients discontinue use and consult a healthcare professional if any of the following occur: the condition worsens, symptoms persist for more than 7 days, symptoms resolve and then recur within a few days, or if excessive skin irritation develops. Additionally, patients should seek medical advice if they experience nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash.

For those using the product for arthritis-related pain, it is important to stop use and consult a doctor if pain persists for more than 10 days or if redness is present. These precautions are essential to ensure patient safety and to address any potential adverse reactions effectively.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Shennong Analgesic Plaster.
Details

Pediatric Use

Pediatric patients under 12 years of age should be advised to contact a healthcare professional before use. This recommendation is crucial to ensure appropriate evaluation and management, as specific dosing and safety considerations may differ in this age group.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

Pregnant patients should not use this medication. The potential risks associated with its use during pregnancy have not been established, and there is insufficient data to determine its safety for fetal outcomes. Healthcare professionals are advised to consider alternative treatments for pregnant women to avoid any potential harm to the developing fetus.

Lactation

Lactating mothers should not use this medication, as it is contraindicated in pregnant women. There is no available data regarding the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, healthcare professionals should exercise caution when considering the use of this medication in lactating mothers.

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, the following management procedures are recommended:

  1. Assessment: Conduct a thorough assessment of the patient's clinical status, including vital signs and level of consciousness.

  2. Supportive Care: Provide supportive care as needed, which may include airway management, oxygen supplementation, and intravenous fluids.

  3. Consultation: Engage with a poison control center or a medical toxicologist for guidance on specific interventions and treatments that may be appropriate based on the substance involved.

  4. Documentation: Document all findings, interventions, and the patient's response to treatment meticulously.

Healthcare professionals should remain vigilant and prepared to implement these general management strategies in the event of an overdose, even in the absence of specific overdosage information.

Nonclinical Toxicology

The use of this product is contraindicated in pregnant women due to potential teratogenic effects. No non-teratogenic effects have been specified in the available data. Additionally, there are no details provided regarding nonclinical toxicology or animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental poisoning. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use the product on wounds, irritated, or damaged skin, except as directed. They should be counseled to stop using the product and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, patients should be advised to discontinue use and seek medical advice if symptoms improve and then recur within a few days.

It is important to inform patients to stop using the product and consult a healthcare professional if they experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash. For those using the product for arthritis pain, they should be instructed to seek medical advice if pain persists for more than 10 days or if redness is present.

Patients should also be cautioned to avoid contact with the eyes or mucous membranes while using this product. Furthermore, they should be advised not to bandage the area tightly when applying the product.

Storage and Handling

The product is supplied in a tightly closed container to maintain its integrity. It should be stored at room temperature, specifically within the range of 20 to 25 °C (68 to 77 °F). Proper storage conditions are essential to ensure the product's efficacy and safety.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Shennong Analgesic Plaster, 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 Shennong Analgesic Plaster, 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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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.