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Gold Bond Medicated Pain and Itch Relief

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Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2023
Label revision date
January 14, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2023
Label revision date
January 14, 2026
Manufacturer
Chattem, Inc.
Registration number
M017
NDC root
41167-0529
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

GOLD BOND Maximum Strength Pain and Itch Relief Cream is a topical cream designed to provide temporary relief from pain and itching caused by various skin issues. You can use it for minor burns, sunburn, minor cuts, scrapes, insect bites, and other minor skin irritations. This cream aims to soothe discomfort and help you feel more comfortable in your skin.

Uses

If you're dealing with minor burns, sunburn, cuts, scrapes, insect bites, or other minor skin irritations, this product can help provide temporary relief from pain and itching. It's designed to soothe your skin and make you feel more comfortable during the healing process.

You can use it for various everyday skin issues, ensuring that you can get back to your activities with less discomfort. Remember, while it’s effective for these minor conditions, it’s always a good idea to consult with a healthcare professional if you have any concerns about your skin or if symptoms persist.

Dosage and Administration

If you are 12 years old or older, you should apply a thin layer of the medication to the affected area. You can do this up to 3 to 4 times each day. Make sure to follow this guideline to ensure the best results.

If you are caring for a child under 12 years of age, it’s important to consult a doctor before using this medication. They can provide the best advice on how to proceed safely.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should not use it in large quantities, especially on raw surfaces or blistered areas, as this can lead to irritation or other complications. Additionally, avoid applying it to deep or puncture wounds, as this could hinder proper healing.

By following these guidelines, you can help ensure that you use the medication effectively and safely. If you have any questions or concerns about its use, please consult your healthcare provider for more information.

Side Effects

When using this product, it's important to apply it only as directed and to avoid contact with your eyes. You should not use it in large amounts, especially on raw or blistered skin, or on deep or puncture wounds. If your condition worsens, if symptoms last more than seven days, or if they improve and then return within a few days, stop using the product and consult a doctor.

Keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center right away.

Warnings and Precautions

This product is for external use only, so please avoid using it on deep or puncture wounds, and do not apply it in large amounts, especially on raw or blistered skin. Always follow the directions on the label carefully and avoid getting the product in your eyes.

If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult your doctor. Additionally, keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center right away.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to seek medical help right away. You can contact a Poison Control Center for guidance.

Signs of an overdose may include unusual symptoms, but specific details about these symptoms are not provided here. If you notice anything concerning, don’t hesitate to get help. Remember, acting quickly can make a difference in ensuring safety and health.

Pregnancy Use

The product has not been specifically evaluated for use during pregnancy, which means there is limited information on its safety for you and your developing baby. However, there are no specific warnings or contraindications noted for pregnant individuals, and no dosage adjustments are recommended if you are pregnant. Additionally, no special precautions are outlined for use during this time.

As always, it's important to discuss any medications or products with your healthcare provider to ensure they are safe for you during pregnancy.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or precautions related to using this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If your child is under 12 years old, it's important to consult a doctor before using this medication. For children aged 12 and older, you can apply a thin layer to the affected area, but be sure to do this no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

While there is no specific information about how this medication should be used by older adults, it’s important to approach any new treatment with caution. Since older adults may have different health needs and may be taking multiple medications, it’s always a good idea to discuss any new prescriptions with your healthcare provider. They can help ensure that the medication is safe and appropriate for you or your loved one, considering any existing health conditions or medications.

If you have concerns about how this medication might affect you or an older adult in your care, please consult with a healthcare professional for personalized advice.

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 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 receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best performance and safety of your product, always remember to close the cap tightly after each use. This simple step helps maintain the integrity of the contents and prevents contamination. Proper handling is essential, so take care to follow this guideline consistently. By doing so, you contribute to the overall effectiveness and safety of the device.

Additional Information

You should apply a thin layer of the medication to the affected area on your skin, using it no more than 3 to 4 times a day if you are an adult or a child aged 12 years and older. If the patient is under 12 years old, it's important to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is GOLD BOND Maximum Strength Pain and Itch Relief Cream used for?

It provides temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.

How should I use this cream?

For adults and children 12 years and older, apply a thin layer to the affected area not more than 3 to 4 times daily. Children under 12 should consult a doctor.

Are there any warnings I should be aware of?

This product is for external use only. Avoid contact with eyes and do not use in large quantities, especially over raw surfaces or on deep or puncture wounds.

What should I do if my condition worsens?

Stop use and ask a doctor if your condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Is this product safe to use during pregnancy?

The product has not been evaluated for use during pregnancy, and there are no specific warnings or contraindications mentioned.

Can nursing mothers use this cream?

There are no specific warnings or precautions mentioned regarding the use of this product by nursing mothers.

What should I do if the cream is swallowed?

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Packaging Info

Below are the non-prescription pack sizes of Gold Bond Medicated Pain and Itch Relief (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Gold Bond Medicated Pain and Itch Relief.
Details

Drug Information (PDF)

This file contains official product information for Gold Bond Medicated Pain and Itch Relief, 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 the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.

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

Dosage and Administration

For adults and children aged 12 years and older, a thin layer of the medication should be applied to the affected area. This application may be performed up to 3 to 4 times daily, depending on the severity of the condition being treated.

For children under 12 years of age, it is recommended to consult a healthcare professional prior to use to determine the appropriate course of action.

Contraindications

Use is contraindicated in the following situations:

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

  • The product should not be applied to deep or puncture wounds, as this may lead to complications or hinder proper healing.

Warnings and Precautions

For external use only. This product should not be applied in large quantities, especially on raw surfaces or blistered areas, and is contraindicated for use on deep or puncture wounds.

When utilizing this product, it is imperative to adhere strictly to the provided directions. Users must read and follow all instructions and warnings indicated on the label. Care should be taken to avoid contact with the eyes, as this may lead to irritation or injury.

In the event that the condition worsens or if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days, it is essential to discontinue use and consult a healthcare professional for further evaluation.

This product must be kept out of reach of children. In the case of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Side Effects

Patients should be aware that this product is for external use only. It is contraindicated for use in large quantities, particularly over raw surfaces or blistered areas, and should not be applied to deep or puncture wounds.

When using this product, it is essential to adhere strictly to the directions provided on the label. Patients should avoid contact with the eyes to prevent irritation.

In the event that the condition worsens, or if symptoms persist for more than 7 days or resolve and then recur within a few days, patients are advised to discontinue use and consult a healthcare professional.

This product should be kept out of reach of children. If ingested, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

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 Gold Bond Medicated Pain and Itch Relief (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Gold Bond Medicated Pain and Itch Relief.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a healthcare professional prior to use. For adolescents and children aged 12 years and older, the recommended application is a thin layer to the affected area, not exceeding 3 to 4 times daily.

Geriatric Use

There is no specific information 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population, given the lack of targeted data.

Pregnancy

The product has not been evaluated for use during pregnancy. There are no specific warnings or contraindications associated with the use of this product in pregnant individuals. Additionally, no dosage modifications are provided for pregnant individuals, and no special precautions regarding use during pregnancy are mentioned. Healthcare professionals should consider the lack of data when prescribing this product to pregnant patients and weigh the potential benefits against any unknown risks.

Lactation

There are no specific warnings or precautions regarding the use of this product by lactating mothers. Additionally, there is no information available concerning the potential for excretion in breast milk or any associated risks to breastfed 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 clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the event of an overdosage, it is imperative to seek immediate medical assistance. Healthcare professionals should advise patients or caregivers to contact a Poison Control Center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved; therefore, monitoring the patient closely for any adverse reactions is essential. Prompt recognition of symptoms can facilitate timely intervention and improve patient outcomes.

Management of overdosage should be guided by the severity of symptoms and the specific agent involved. Healthcare providers are encouraged to follow established protocols for the treatment of overdosage, which may include supportive care and symptomatic treatment as necessary.

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 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 informed not to use the product in large quantities, especially over raw surfaces or blistered areas, and to avoid application on deep or puncture wounds. It is important to instruct patients to stop using the product and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms clear up and then recur within a few days, patients should also seek medical advice.

Healthcare providers should emphasize the importance of using the product only as directed, and patients should be encouraged to read and follow all directions and warnings on the label. Lastly, patients should be cautioned to avoid contact with their eyes while using this product.

Storage and Handling

The product is supplied in a configuration that requires careful handling to maintain its integrity. It is essential to ensure that the cap is closed tightly between uses to prevent contamination and preserve the product's efficacy.

For optimal storage, the product should be kept in a controlled environment, away from extreme temperatures. Specific temperature ranges and container requirements are not provided; however, general best practices for storage should be followed to ensure product stability and safety.

Additional Clinical Information

The medication is administered topically. For adults and children aged 12 years and older, a thin layer should be applied to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a doctor prior to use. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Gold Bond Medicated Pain and Itch 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 Gold Bond Medicated Pain and Itch 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.