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Dr Tatty Numbing

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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)
Marketed in the U.S.
Since 2025
Label revision date
September 17, 2025
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
Marketed in the U.S.
Since 2025
Label revision date
September 17, 2025
Manufacturer
Prodigy Media Inc
Registration number
M017
NDC root
70171-0020

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If you are a consumer or patient please visit this version.

Drug Overview

Dr Tatty Numbing Cream is a topical product designed to provide temporary relief from pain and itching caused by various skin issues, including sunburns, minor cuts, insect bites, and skin irritations. This cream can help soothe discomfort and promote a sense of relief when you experience these common skin problems.

While the specific mechanism of action is not detailed, its primary purpose is to alleviate the discomfort associated with these conditions, making it a useful option for managing minor skin irritations.

Uses

If you're dealing with discomfort from sunburns, minor cuts, insect bites, or skin irritations, this medication can help provide temporary relief from pain and itching. It's designed to soothe your skin and make you feel more comfortable during these minor irritations.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

If you are an adult or a child aged 2 years and older, you can apply this medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results. However, if the person needing treatment is under 2 years old, it’s important not to use this medication without first consulting a physician (doctor). Always prioritize safety and seek professional advice when it comes to young children.

What to Avoid

You can feel confident using this medication, as there are no specific contraindications (conditions that would make the use of the drug inadvisable) listed. Additionally, there are no concerns regarding its classification as a controlled substance, risks of abuse or misuse, or issues related to dependence (a condition where the body becomes reliant on a substance).

Since there are no specific "do not take" or "do not use" instructions provided, it appears to be safe for you to use as directed. Always remember to follow your healthcare provider's guidance and reach out if you have any questions or concerns about your treatment.

Side Effects

When using this product, it's important to be aware of some potential side effects. You should stop using it and consult a doctor if your condition worsens or if symptoms last longer than 7 days. If your symptoms improve but then return within a few days, it's also advisable to seek medical advice. Additionally, avoid using this product on wounds or damaged skin, and do not apply it in large amounts, especially on raw or blistered areas. Always follow the recommended dosage unless directed otherwise by a healthcare professional.

Warnings and Precautions

This product is for external use only, so please avoid contact with your eyes. It's important to stop using it and consult your doctor if your condition worsens or if symptoms last longer than 7 days. Additionally, if your symptoms improve and then return within a few days, you should also reach out to your doctor. Be cautious not to use large amounts, especially on raw or blistered skin, and do not apply it to wounds or damaged areas.

If you accidentally swallow the product, seek emergency medical help or contact a Poison Control Center immediately. Always follow the recommended dosage and guidelines to ensure your safety.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's important to be aware of the general signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it is crucial to seek immediate medical help.

In case of an emergency, you should call your local emergency number or go to the nearest hospital. Always keep your medications in a safe place and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of lidocaine HCL cream during pregnancy has not been established. There may be potential risks to your fetus, so you should approach the use of this cream with caution. Always consult your physician before using it to ensure it is safe for your specific situation.

Additionally, if you do use lidocaine HCL cream while pregnant, your healthcare provider may recommend dosage adjustments. It's essential to seek their guidance to ensure both your safety and the safety of 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 it may pose to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

When using this product for children aged 2 years and older, you can apply it to the affected area up to 3 to 4 times a day. However, if your child is under 2 years old, it's important not to use this product without first consulting a physician (a medical doctor). Always keep the product out of reach of children to prevent accidental ingestion.

If the product is swallowed, seek medical help immediately or contact a Poison Control Center for assistance. Your child's safety is the top priority, so please follow these guidelines carefully.

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 considering this medication, it’s important to consult with a healthcare provider. 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, especially as you navigate the complexities of aging and medication management.

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 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. 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 of your product, store it at room temperature. It's important to check the packaging before use; do not use the product if the seal is broken, as this could compromise its safety and effectiveness. By following these simple guidelines, you can help maintain the integrity of the product and ensure safe usage.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged 2 years and older. If the patient is under 2 years of age, it's important to consult a physician before use. There are no additional details available regarding laboratory tests, abuse potential, or postmarketing experiences related to this medication.

FAQ

What is Dr Tatty Numbing Cream used for?

Dr Tatty Numbing Cream is used for the temporary relief of pain and itching associated with sunburns, minor cuts, insect bites, and skin irritations.

How should I apply Dr Tatty Numbing Cream?

Adults and children 2 years of age and older should apply it to the affected area no more than 3 to 4 times daily. Children under 2 years of age should not use it and should consult a physician.

Are there any warnings for using Dr Tatty Numbing Cream?

Yes, it is for external use only, and you should avoid contact with eyes. Stop use and ask a doctor if the condition worsens or symptoms persist for more than 7 days.

Can I use Dr Tatty Numbing Cream if I am pregnant?

The safety of Dr Tatty Numbing Cream during pregnancy has not been established. Consult a physician before use if you are pregnant or planning to become pregnant.

What should I do if I swallow Dr Tatty Numbing Cream?

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

Is there any information about using Dr Tatty Numbing Cream while nursing?

There are no specific warnings or recommendations regarding the use of this product in nursing mothers.

How should I store Dr Tatty Numbing Cream?

Store Dr Tatty Numbing Cream at room temperature and do not use it if the seal is broken.

Packaging Info

Below are the non-prescription pack sizes of Dr Tatty Numbing (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr Tatty Numbing.
Details

Drug Information (PDF)

This file contains official product information for Dr Tatty Numbing, 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 sunburns, minor cuts, insect bites, and skin irritations.

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

Dosage and Administration

For adults and children aged 2 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. It is important to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

For children under 2 years of age, the product should not be used without consulting a physician. Healthcare professionals are advised to evaluate the necessity and safety of treatment in this age group before proceeding with any application.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes. In the event that the condition worsens or symptoms persist for more than 7 days, the patient should discontinue use and consult a healthcare professional. Additionally, if symptoms resolve and then recur within a few days, the patient is advised to stop use and seek medical advice.

The product should not be applied in large quantities, especially over raw surfaces or blistered areas, and the recommended daily dosage should not be exceeded unless directed by a physician. It is also contraindicated for use on wounds or damaged skin.

In cases where the product is ingested, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Patients should be instructed to stop using the product and consult their doctor if the condition worsens or if symptoms persist beyond 7 days. Furthermore, if symptoms improve and then reappear within a short timeframe, it is essential to cease use and seek medical evaluation.

Side Effects

Patients should be aware that the product is for external use only and must avoid contact with the eyes. It is crucial to stop use and consult a doctor if the condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms clear up and then recur within a few days, medical advice should be sought.

Patients are advised against using the product in large quantities, particularly over raw surfaces or blistered areas, and should not exceed the recommended daily dosage unless directed by a healthcare professional. Furthermore, the product should not be applied to wounds or damaged skin to prevent potential adverse reactions.

Drug Interactions

There are currently no documented drug interactions associated with 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 Dr Tatty Numbing (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr Tatty Numbing.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the product to the affected area up to 3 to 4 times daily. For children under 2 years of age, the product is not recommended, and consultation with a physician is advised. It is important to keep the product out of reach of children. In the event of accidental ingestion, medical assistance should be sought immediately, or contact a Poison Control Center.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

The safety of lidocaine HCL cream during pregnancy has not been established. Pregnant patients or those planning to become pregnant should consult a physician before use. There may be potential risks to the fetus; therefore, the use of this medication should be approached with caution. Additionally, dosage adjustments may be necessary for pregnant individuals, and it is recommended to consult a healthcare provider for guidance on appropriate dosing.

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.

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 overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, altered mental status, cardiovascular instability, or gastrointestinal disturbances.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. Healthcare professionals should also consider contacting a poison control center for additional guidance on the management of overdose cases.

In summary, while specific overdosage information is not available, prompt recognition and appropriate management of overdose symptoms are critical in ensuring patient safety.

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.

Patient Counseling

Healthcare providers should advise patients that if the product is swallowed, it is crucial to seek medical help immediately or contact a Poison Control Center. This information is essential for ensuring patient safety and prompt action in case of accidental ingestion.

Storage and Handling

The product is supplied in configurations that include specific NDC numbers, which should be referenced for accurate identification. It is essential to store the product at room temperature to maintain its integrity and efficacy. Additionally, the product must not be used if the seal is broken, as this may compromise its safety and effectiveness. Proper handling and storage conditions are crucial to ensure the product remains suitable for use.

Additional Clinical Information

The medication is administered topically, with the recommended application frequency for adults and children aged 2 years and older being 3 to 4 times daily to the affected area. For children under 2 years of age, it is advised to consult a physician before 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 Dr Tatty Numbing, 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 Dr Tatty Numbing, 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.