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701 Dieda Zhengtong Yaogao Medicated

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This product has been discontinued

Active ingredients
  • Camphor (synthetic) 3.1 g
  • Menthol 8 g
  • Methyl Salicylate 10 g
Other brand names
Dosage form
Plaster
Routes
  • Topical
  • Transdermal
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2001
Label revision date
November 13, 2019
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 3.1 g
  • Menthol 8 g
  • Methyl Salicylate 10 g
Other brand names
Dosage form
Plaster
Routes
  • Topical
  • Transdermal
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 2001
Label revision date
November 13, 2019
Manufacturer
GUANGZHOU BAIYUNSHAN PHARMACEUTICAL CO. , LTD. BAIYUNSHAN HEJIGONG PHARMACEUTICAL FACTORY
Registration number
part348
NDC root
61822-0046
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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Drug Overview

701 DIEDA ZHENGTONG YAOGAO MEDICATED PLASTER is an external analgesic designed to provide temporary relief from minor aches and pains in muscles and joints. You can use it for conditions such as simple backache, arthritis, strains, bruises, and sprains. This medicated plaster works by delivering soothing ingredients directly to the affected area, helping to alleviate discomfort and promote mobility.

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 this treatment to ease discomfort and help you get back to your daily activities. Remember, it's designed for short-term use to alleviate those nagging pains.

Dosage and Administration

To use this medication effectively, start by cleaning the area of skin that needs treatment. Once the area is clean, carefully remove the paper film from the plaster.

For adults and children aged 12 years and older, you can apply one plaster to the affected area up to three to four times a day. However, if the patient is under 12 years old, it’s important not to use this medication without first consulting a physician, as using it incorrectly can be dangerous. Always follow these guidelines to ensure safe and effective use.

What to Avoid

You should avoid using this product if you have irritated or damaged skin, on any wounds, or if you are pregnant or nursing. It's also important not to use it with a heating pad or in any way other than as directed.

While using this product, make sure to keep it away from your eyes and mucous membranes, and avoid wrapping or bandaging the area tightly. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

This product contains natural rubber latex, which may cause allergic reactions in some individuals. If you experience any signs of an allergy, such as rash or difficulty breathing, seek medical attention immediately.

You should stop using this product and consult a doctor if your condition worsens, if symptoms last longer than 7 days, or if they improve and then return within a few days. Additionally, if you notice excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash, it's important to reach out to a healthcare professional. For those using it for arthritis pain, contact your doctor if the pain continues for more than 10 days or if you see any redness. Special caution is advised for children under 12 years of age.

Warnings and Precautions

This product is for external use only and contains natural rubber latex, which can cause allergic reactions in some people. Please avoid using it on irritated or damaged skin, open wounds, or in combination with a heating pad. If you are pregnant or nursing, or if you plan to use it in any way other than as directed, it’s best to refrain from using this product.

You should stop using the product and contact your doctor if your condition worsens, if symptoms last longer than 7 days, or if they clear up and then return within a few days. Additionally, seek medical advice if you experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash. For those using it for arthritis pain, if the pain persists for more than 10 days or if redness is present, consult your doctor. This product is not recommended for children under 12 years of age.

If the product is swallowed, 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 effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe you have taken too much of the medication, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get checked out if you have any concerns about your health.

Pregnancy Use

If you are pregnant or nursing, it is important to avoid using this medication. The potential risks to your baby during pregnancy or while breastfeeding are significant, and it is best to prioritize your health and the health of your child. Always consult with your healthcare provider for guidance on safe medication use during this time.

Lactation Use

If you are breastfeeding, it is important to know that this medication should not be used while you are nursing. Using it during this time could pose risks to your baby. Always consult with your healthcare provider for guidance on safe medications while breastfeeding to ensure the well-being of both you and your infant.

Pediatric Use

If your child is under 12 years old, it's important not to use this product without first consulting a physician. Using it incorrectly can be dangerous for younger children. For those aged 12 and older, you can apply one plaster to the affected area, but make sure not to exceed 3 to 4 applications in a day.

Always check with a healthcare professional if your child has any conditions that might require treatment, especially if they are under 12 years of age. Their safety and well-being should always come first.

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 always wise to discuss any medications with a healthcare provider, especially since older adults may have different health needs and may be taking other medications.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health conditions and overall treatment goals. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

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 detailed recommendations available for how your liver health might affect the use of this medication.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and appropriate for your liver condition. They can help you understand how to manage your health effectively while using this medication.

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 any concerns you may have regarding your medications or tests. Your safety and well-being are the top priorities, and clear communication is key to achieving the best outcomes.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a tightly closed container. It's important to keep it at room temperature, ideally between 15º to 30º C (59º to 86º F), and away from direct sunlight. This will help maintain its quality and prevent any degradation.

When handling the product, always ensure that your hands are clean and that you are in a safe environment to avoid contamination. Following these guidelines will help you use the product safely and effectively.

Additional Information

You can use this medication by applying one plaster to the affected area on your skin. For adults and children aged 12 years and older, you can apply the plaster up to 3 to 4 times a day. However, if the patient is under 12 years old, it's important to consult a physician before use.

There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is 701 DIEDA ZHENGTONG YAOGAO MEDICATED PLASTER used for?

It is an external analgesic 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 use the plaster?

Clean the affected area, remove the paper film from the plaster, and apply one plaster to the affected area not more than 3 to 4 times daily for adults and children 12 years and older.

Are there any contraindications for using this plaster?

Yes, do not use it on irritated or damaged skin, wounds, or with a heating pad. It should not be used if you are pregnant or nursing.

What should I do if I experience adverse reactions?

Stop use and ask a doctor if your condition worsens, symptoms persist for more than 7 days, or if you experience excessive skin irritation, nausea, or other serious symptoms.

Is this product safe for children?

Children under 12 years of age should not use this plaster without consulting a physician, as it may be dangerous.

What precautions should I take when using this product?

Avoid contact with eyes or mucous membranes, do not bandage tightly, and ensure you do not use it otherwise than as directed.

What should I do if I accidentally swallow the plaster?

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

How should I store the plaster?

Keep it in a tightly closed container at room temperature, between 15º to 30º C (59º to 86º F), away from sunlight.

Packaging Info

Below are the non-prescription pack sizes of 701 Dieda Zhengtong Yaogao Medicated (camphor, menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for 701 Dieda Zhengtong Yaogao Medicated.
Details

Drug Information (PDF)

This file contains official product information for 701 Dieda Zhengtong Yaogao Medicated, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

701 DIEDA ZHENGTONG YAOGAO MEDICATED PLASTER is an external analgesic available in two packaging formats. The first format contains one plaster measuring 3.9 x 157 inches (10 x 400 cm), while the second format includes ten plasters, each measuring 4 x 2.8 inches (10 x 7 cm). The product is identified by the National Drug Code (NDC) 61822-0046-1 for the single plaster and NDC 61822-0046-2 for the ten plaster package.

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 thoroughly prior to application. After cleaning, the paper film must be removed from the plaster.

For adults and children aged 12 years and older, one plaster should be applied to the affected area, with a maximum frequency of 3 to 4 times daily.

For children under 12 years of age, the use of this product is not recommended. Consultation with a physician is advised, as use in this population may pose risks if not directed appropriately.

Contraindications

Use of this product is contraindicated in the following situations:

The product should not be applied to irritated or damaged skin, as this may exacerbate the condition. It is also contraindicated for use on open wounds due to the risk of infection and delayed healing. The application of this product in conjunction with a heating pad is prohibited, as it may lead to increased skin irritation or burns.

Additionally, the product is contraindicated for use in pregnant or nursing individuals due to potential risks to the fetus or infant. It must be used strictly as directed; any deviation from the recommended usage is not advised.

Contact with the eyes or mucous membranes should be avoided, and tight bandaging is not recommended during use.

Warnings and Precautions

For external use only. This product contains natural rubber latex, which may cause allergic reactions in sensitive individuals.

It is imperative to adhere to the following precautions to ensure safe use. The product should not be applied to irritated or damaged skin, nor should it be used on open wounds. Additionally, the use of heating pads in conjunction with this product is contraindicated. Pregnant or nursing individuals should refrain from using this product, and it should only be used as directed.

Healthcare professionals should advise patients to discontinue use and consult a physician 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; excessive skin irritation develops; gastrointestinal symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash manifest; in cases of arthritis pain, if pain persists for more than 10 days or if redness is present; or if the product is being used for children under 12 years of age.

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

Side Effects

Patients using this product should be aware of the potential for allergic reactions, particularly due to the presence of natural rubber latex, which may elicit allergic responses in susceptible individuals.

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, excessive skin irritation develops, or gastrointestinal symptoms such as nausea, vomiting, abdominal discomfort, diarrhea, or skin rash manifest.

For patients utilizing this product for arthritis-related pain, it is particularly important to seek medical advice if pain persists for more than 10 days or if redness is observed. Additionally, caution is advised when administering this product to children under 12 years of age, as specific adverse reactions may be more pronounced in this population.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of 701 Dieda Zhengtong Yaogao Medicated (camphor, menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for 701 Dieda Zhengtong Yaogao Medicated.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this product without consulting a physician, as use otherwise than directed may pose risks. For adolescents and children aged 12 years and older, the recommended dosage is to apply one plaster to the affected area no more than 3 to 4 times daily. In cases involving conditions affecting pediatric patients under 12 years, it is essential to seek medical advice.

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 potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Pregnant patients and those who are nursing should not use this medication. The potential risks associated with the use of this drug during pregnancy have not been established, and its safety profile in this population remains unclear. Therefore, healthcare professionals are advised to consider alternative treatments for women who are pregnant or breastfeeding.

Lactation

Lactating mothers should not use this medication while nursing. There is no available data on the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, caution is advised, and alternative treatments should be considered for 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 this medication. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions recommended for individuals with compromised liver function. It is advised that healthcare professionals exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population.

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, as the clinical presentation can vary depending on the substance involved and the individual patient's response. Common symptoms of overdose may include, but are not limited to, altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of an overdose, immediate medical intervention is recommended. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and ensuring adequate circulation. The use of activated charcoal may be considered if the patient presents within a suitable timeframe and is deemed appropriate based on clinical judgment.

Additionally, it is crucial to consult local poison control centers or toxicology experts for guidance on specific management strategies tailored to the substance involved in the overdose. Continuous monitoring and supportive care should be maintained until the patient is stabilized and any potential complications are addressed.

Documentation of the incident, including the substance involved, estimated dose, time of ingestion, and any symptoms observed, is vital for ongoing management and future reference.

Nonclinical Toxicology

The use of this product is contraindicated in pregnant or nursing individuals 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 provided data.

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 irritated or damaged skin, on wounds, or in conjunction with a heating pad. Additionally, it is important to counsel patients against using the product if they are pregnant or nursing, and to use it only as directed.

Patients should be instructed to stop using the product 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. They should also be advised to seek medical attention if they experience excessive skin irritation, nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash.

For those using the product for arthritis pain, it is crucial to inform them to stop use and consult a doctor if the pain persists for more than 10 days. Patients should also be cautioned to seek medical advice if redness is present or if they are treating conditions affecting children under 12 years of age.

When using this product, patients should avoid contact with the eyes or mucous membranes and should not bandage the area tightly.

Storage and Handling

The product is supplied in a tightly closed container to ensure its integrity. It should be stored at room temperature, specifically within the range of 15º to 30º C (59º to 86º F). Care should be taken to keep the product away from direct sunlight to maintain its quality and effectiveness.

Additional Clinical Information

The medication is administered topically via transdermal application. For adults and children aged 12 years and older, one plaster should be applied to the affected area no more than 3 to 4 times daily. It is advised that children under 12 years of age should not use this medication and should consult a physician for guidance.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for 701 Dieda Zhengtong Yaogao Medicated, 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 701 Dieda Zhengtong Yaogao Medicated, 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.