Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Gold Bond Medicated Pain and Itch Relief

Last content change checked dailysee data sync status

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
December 4, 2025
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
December 4, 2025
Manufacturer
Gold Bond Co LLC
Registration number
M017
NDC root
84714-0529
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

GoldBond Pain & Itch Relief Cream is designed to provide temporary relief from pain and itching caused by various skin conditions. 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

You can use this medication for temporary relief from pain and itching caused by various skin issues. It is effective for minor burns, sunburn, minor cuts, scrapes, insect bites, and other minor skin irritations.

This product is designed to help soothe discomfort and promote healing, making it a handy option for everyday skin mishaps. Remember, it’s always a good idea to consult with a healthcare professional if you have any concerns about your skin or the use of this medication.

Dosage and Administration

When using this medication, you should apply a thin layer to the affected area. For adults and children aged 12 years and older, you can do this up to 3 to 4 times each day. It's important not to exceed this frequency to ensure safe and effective use.

If the patient is a child under 12 years old, it's essential to consult a doctor before applying the medication. This will help ensure that the treatment is appropriate and safe for younger patients. Always follow your healthcare provider's guidance for the best results.

What to Avoid

It's important to use this medication safely to avoid potential complications. You should not use it in large quantities, especially on raw or blistered areas, and avoid applying it to deep or puncture wounds. Additionally, make sure to keep it away from your eyes, as contact can cause irritation or harm.

If you have any concerns about misuse or dependence (which refers to a condition where you may feel a strong need to use a substance), please discuss them with your healthcare provider. Your safety is a priority, so following these guidelines is essential for effective and safe use.

Side Effects

When using this product, it's important to apply it only as directed and avoid contact with your eyes. You should not use it in large amounts, especially on raw or blistered areas, or on deep or puncture wounds. If your condition worsens, if symptoms last more than 7 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 swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

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

If your condition worsens, or if symptoms last longer 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 a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there are no specific warnings or precautions associated with the use of this product during pregnancy. The information available does not indicate any risks to the fetus or any contraindications for pregnant individuals. Additionally, there are no dosage modifications recommended for those who are pregnant, and no special precautions are noted for its use during this time.

As always, it's best to consult with your healthcare provider about any medications you are considering or currently using while pregnant to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of 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 associated with its use during lactation. 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 those 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 safe and effective use for your child.

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. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

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 any 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 differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual’s health situation is unique, and your healthcare provider can help ensure that your treatment is safe and effective. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. It's important to keep it out of reach of children to prevent accidental ingestion. Always remember to close the cap tightly after each use to maintain its integrity. The product comes in child-resistant packaging, adding an extra layer of safety for households with young ones. By following these simple guidelines, you can help ensure that the product remains safe and effective for your use.

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 GoldBond Pain & Itch Relief Cream used for?

GoldBond Pain & Itch Relief Cream 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 GoldBond Pain & Itch Relief 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. For children under 12, consult a doctor.

Are there any warnings for using this cream?

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

What should I do if my condition worsens or does not improve?

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 GoldBond Pain & Itch Relief Cream safe to use during pregnancy?

There are no specific warnings or precautions mentioned regarding the use of this product during pregnancy.

Can nursing mothers use this cream?

The insert does not provide specific warnings or recommendations regarding the use of this product in nursing mothers.

How should I store GoldBond Pain & Itch Relief Cream?

Store at room temperature, keep out of reach of children, and close the cap tightly between uses.

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 specified 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.

In the case of children under 12 years of age, it is advised to consult a healthcare professional for appropriate dosing and administration guidance.

Contraindications

Use is contraindicated in the following situations:

Application in large quantities, particularly over raw surfaces of blistered areas, is not recommended due to the potential for increased irritation and adverse effects. Additionally, the product should not be applied to deep or puncture wounds, as this may lead to complications or delayed healing.

Contact with the eyes must be avoided, as it can result in significant irritation or injury.

Warnings and Precautions

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

When using this product, it is imperative to adhere strictly to the directions provided. Users must read and follow all instructions and warnings indicated on the carton. Care should be taken to avoid contact with the eyes.

If the condition worsens, or if symptoms persist for more than 7 days or resolve only to recur within a few days, it is essential to discontinue use and consult a healthcare professional.

This product must be kept out of reach of children. In the event 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 of 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. Patients are advised to read and follow all instructions and warnings on the carton carefully. Additionally, contact with the eyes should be avoided to prevent irritation.

Patients should discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days.

This product should be kept out of reach of children. In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

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 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 doctor before 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

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

Pregnancy

There are no specific warnings or precautions regarding the use of this product during pregnancy. The prescribing information does not provide any data on the risk to the fetus or contraindications associated with its use in pregnant patients. Additionally, no dosage modifications for pregnant individuals are specified. The insert also does not mention any special precautions for use during pregnancy. Healthcare professionals should consider the absence of data when advising women of childbearing potential and pregnant patients regarding the use of this product.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants during the use of this product.

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 event of an overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous monitoring and evaluation are recommended to ensure patient safety and effective resolution of any complications arising from the overdosage.

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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

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

Patients should be cautioned against using the product in large quantities, especially on raw surfaces of blistered areas, and it should not be applied to deep or puncture wounds. It is important to inform patients 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 seek medical advice if symptoms clear up and then recur within a few days.

When using this product, patients must be reminded to follow all directions and warnings provided on the carton carefully. They should also be informed to avoid contact with the eyes during application.

Storage and Handling

This product is supplied in child-resistant packaging to ensure safety. It should be stored at room temperature, away from direct sunlight and moisture. To maintain product integrity, the cap must be closed tightly between uses. Additionally, it is important to keep this product out of reach of children to prevent accidental ingestion.

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 additional 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.