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Green Guard Topical Pain Relief

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Active ingredient
Lidocaine Hydrochloride 20 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2020
Label revision date
April 7, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 20 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Spray
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 2020
Label revision date
April 7, 2025
Manufacturer
Ultra Distributors Inc
Registration number
M017
NDC root
78495-132
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

If you are experiencing minor burns, there is a medication designed to provide temporary pain relief. This drug works specifically to alleviate the discomfort associated with these types of injuries, helping you feel more comfortable as you heal. While the exact mechanism of action isn't detailed, its primary purpose is to ease the pain you may be feeling from minor burns.

Uses

If you’re dealing with minor burns, this medication can provide you with temporary relief from the pain associated with those injuries. It’s designed to help ease your discomfort, allowing you to go about your day with less irritation.

Rest assured, this medication does not have any known teratogenic effects, meaning it does not cause harm to a developing fetus. This makes it a safer option for those who may be pregnant or planning to become pregnant.

Dosage and Administration

To use the burn spray effectively, start by cleaning the affected area thoroughly. Once it’s clean, spray an even layer of the burn spray over the area. You can do this up to 3 to 4 times a day, depending on your needs.

Please note that this product is not suitable for children under 12 years of age, so make sure to keep it out of reach of younger kids. Always follow these guidelines to ensure safe and effective use of the spray.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should not apply it in large amounts, especially on raw or blistered skin, as this can lead to irritation or other complications. Additionally, be careful not to use it near your eyes; if it does come into contact with your eyes, rinse them thoroughly with water to prevent discomfort.

While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this product, following these guidelines will help ensure your safety and well-being.

Side Effects

It's important to note that this product is for external use only. If you notice that your condition worsens or does not improve after 7 days, or if it seems to clear up and then comes back, you should stop using the product and consult a doctor.

Warnings and Precautions

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

You should stop using this product and call your doctor if your condition worsens, persists for more than 7 days, or if it seems to improve and then returns. It's important to monitor your symptoms closely and take action if necessary.

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 unsure, 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 checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Pregnancy Use

When considering the use of GREEN GUARD TOPICAL PAIN RELIEF (lidocaine hci spray) during pregnancy, it's important to note that there is no available information about its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that the effects of this product on you or your developing baby are not well understood.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before using any medication, including topical treatments like this one. They can help you weigh the potential risks and benefits based on your specific situation.

Lactation Use

If you are breastfeeding, it's important to be aware that some substances can be passed into your breast milk. This means that anything you take could potentially affect your nursing infant. Because there haven't been specific studies on how this product impacts breastfeeding babies, it's best to exercise caution when using it. Always consult with your healthcare provider to ensure the safety of both you and your child while breastfeeding.

Pediatric Use

It's important to know that this medication should not be used in children under 12 years of age. If you have a child in this age group, please consult your healthcare provider for alternative options that are safe and appropriate for their age. Always prioritize your child's health and follow medical advice regarding their treatment.

Geriatric Use

It's important to note that this medication is not intended for children under 12 years of age. For older adults, there are no specific dosage adjustments or safety concerns mentioned in the available information. This means that, generally, you can use the medication as directed without special precautions related to age. However, always consult with a healthcare provider to ensure it’s appropriate for your individual health needs.

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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments 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 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 regarding your liver function and how it relates to your treatment. They can help ensure that your medication 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 any other medications or supplements you may be using. This helps to create a comprehensive picture of your health and ensures your safety while receiving treatment.

Storage and Handling

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

When handling the product, be sure to do so with clean hands and in a sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

You should apply the burn spray topically by spraying an even layer over the cleaned affected area. It is recommended to do this no more than 3 to 4 times a day for optimal results. There are no additional details regarding laboratory tests, abuse potential, or patient counseling information available at this time.

FAQ

What is the primary use of this drug?

This drug is used for temporary pain relief associated with minor burns.

How should I apply the burn spray?

You should spray an even layer of the burn spray over the cleaned affected area no more than 3-4 times daily.

Is this drug safe for children?

This drug should not be used on children under 12 years of age.

What should I do if the condition worsens?

You should stop using the product and ask a doctor if the condition worsens or persists for more than 7 days.

Are there any warnings I should be aware of?

Yes, this product is for external use only and should not be used in large quantities, especially over raw or blistered areas.

Can I use this drug while pregnant?

There is no specific information regarding the use of this drug during pregnancy.

Is it safe to use while breastfeeding?

Caution is advised while breastfeeding due to the potential for excretion in breast milk.

What should I do if I accidentally swallow the spray?

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

What is the recommended storage temperature for this drug?

You should store this drug at 68°-77°F (20°-25°C).

Packaging Info

Below are the non-prescription pack sizes of Green Guard Topical Pain Relief (lidocaine hci). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Green Guard Topical Pain Relief.
Details

Drug Information (PDF)

This file contains official product information for Green Guard Topical Pain Relief, 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 available data.

Uses and Indications

This drug is indicated for the temporary relief of pain associated with minor burns.

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

Dosage and Administration

Healthcare professionals are advised to apply an even layer of the burn spray to the cleaned affected area. This application should not exceed 3 to 4 times daily.

It is important to note that this product is contraindicated for use in children under 12 years of age.

Contraindications

Use is contraindicated in the following situations:

  • Application in large quantities, particularly over raw or blistered areas, is not recommended due to the potential for increased irritation or adverse effects.

  • Avoid application near the eyes; in the event of contact, rinse thoroughly with water to prevent irritation or injury.

Warnings and Precautions

For external use only. It is imperative that healthcare professionals advise patients to adhere strictly to this guideline to prevent any adverse effects associated with inappropriate use.

In the event of accidental ingestion, immediate medical assistance should be sought. Patients should be instructed to contact a Poison Control Center or seek medical help without delay to ensure appropriate management of potential toxicity.

Healthcare providers should monitor patients closely and advise them to discontinue use and consult a physician if their condition worsens, persists for more than 7 days, or if symptoms resolve and then recur. This vigilance is essential to ensure patient safety and effective management of their condition.

Side Effects

For external use only. Patients should discontinue use and consult a doctor if the condition worsens, persists for more than 7 days, or if the condition clears up and then returns.

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 Green Guard Topical Pain Relief (lidocaine hci). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Green Guard Topical Pain Relief.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this medication. Safety and efficacy have not been established in this population, and therefore, it is contraindicated for children in this age group. Healthcare professionals are advised to consider alternative treatments for pediatric patients under 12.

Geriatric Use

Elderly patients, defined as those aged 65 years and older, have not been specifically addressed in terms of dosage adjustments or safety considerations in the available prescribing information. There are no noted safety concerns or special precautions for this population. Additionally, the medication is contraindicated for use in children under 12 years of age.

Healthcare providers should continue to monitor elderly patients as they would for any other demographic, given the absence of specific geriatric use data.

Pregnancy

There is currently no information available regarding the use of GREEN GUARD TOPICAL PAIN RELIEF (lidocaine hci spray) during pregnancy. This includes a lack of data on safety concerns, dosage modifications, or any special precautions that should be taken when considering the use of this medication in pregnant patients. Healthcare professionals are advised to weigh the potential benefits against any unknown risks when prescribing this medication to women of childbearing potential. Given the absence of specific data, caution is recommended in the use of this product during pregnancy.

Lactation

Nursing mothers should be aware of the potential for excretion of this product in breast milk. Caution is advised when using this product while breastfeeding due to the lack of specific studies on its effects on nursing 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 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, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the substance involved, estimated dose, and time of exposure, is crucial for effective management and follow-up care.

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 these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients that in the event of accidental ingestion, it is crucial to seek medical assistance immediately or contact a Poison Control Center. This 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 at a controlled temperature range of 68° to 77°F (20° to 25°C) to maintain its integrity and efficacy. Proper storage conditions should be ensured to prevent any degradation of the product.

Additional Clinical Information

The product is administered topically, with instructions for patients to spray an even layer of the burn spray over the cleaned affected area. This application should not exceed 3-4 times daily.

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 Green Guard Topical Pain Relief, 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 Green Guard Topical Pain Relief, 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.