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Inkkulture 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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
September 17, 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 2025
Label revision date
September 17, 2025
Manufacturer
Prodigy Media Inc
Registration number
M017
NDC root
70171-0022
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

INK Kulture LIDO Cream is a topical medication 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 works by numbing the affected area, helping to soothe discomfort and promote a sense of relief.

If you're dealing with any of these skin conditions, INK Kulture LIDO Cream may be a helpful option to consider for alleviating your symptoms. Always remember to follow the instructions for use to ensure the best results.

Uses

You can use this medication for the temporary relief of pain and itching caused by sunburns, minor cuts, insect bites, and various skin irritations. It helps soothe discomfort and provides a sense of relief when your skin is feeling irritated or damaged.

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 your child 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 younger children.

What to Avoid

It's important to be aware of specific instructions regarding the use of this product. If you accidentally swallow it, seek medical help immediately or contact a Poison Control Center. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this product. However, always prioritize your health and follow the guidance provided.

Side Effects

You should be aware that this product is for external use only and should not come into contact with your eyes. If your condition worsens or symptoms last longer than 7 days, it's important to stop using the product and consult a doctor. Additionally, if your symptoms improve and then return within a few days, you should also seek medical advice. Avoid using large amounts, especially on raw or blistered skin, and do not exceed the recommended daily dosage unless directed by a healthcare professional. Lastly, do not apply this product to wounds or damaged skin.

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 healthcare provider. 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, if you suspect that you or someone else may have taken too much of a medication, it’s important to be aware of potential signs of an overdose, which can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms, or if you are unsure whether an overdose has occurred, seek immediate medical help. You can contact your local emergency services or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any risk of overdose.

Pregnancy Use

The safety of lidocaine HCL cream during pregnancy has not been established, which means that it’s unclear whether it could harm you or your developing baby. It is generally not recommended to use this cream while pregnant unless your healthcare provider believes that the benefits outweigh the potential risks to your fetus.

If you are pregnant and considering using lidocaine HCL cream, it’s important to consult your physician first. They may suggest dosage adjustments to ensure safety. Always prioritize open communication with your healthcare provider about any medications you are considering during pregnancy.

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 medication 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 medication without first consulting a physician (a medical doctor). Always prioritize your child's safety and seek professional advice if you have any concerns.

Geriatric Use

When it comes to using INKKULTURE NUMBING (lidocaine hcl cream), there are no specific guidelines or dosage adjustments for older adults. This means that, based on the information available, you can use this cream without special considerations related to age. However, it's always a good idea to consult with your healthcare provider before starting any new medication, especially if you have other health conditions or are taking multiple medications. They can help ensure that this treatment is safe and effective for your individual 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. This means that there are no tailored recommendations for how your kidney condition 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 effective for your specific situation. They can help determine the best approach based on your kidney health.

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 if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

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 share your complete list of medications and any health conditions you have to receive the best care possible.

Storage and Handling

To ensure the best performance and safety 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. Always handle the product with care to maintain its integrity.

Additional Information

For adults and children aged 2 years and older, you should apply the medication to the affected area no more than 3 to 4 times a day. If the patient is under 2 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 INK Kulture LIDO Cream used for?

INK Kulture LIDO 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 INK Kulture LIDO Cream?

Adults and children 2 years of age and older should apply it to the affected area not 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 contraindications for using this cream?

There are no contraindications listed for INK Kulture LIDO Cream, but it should not be used on wounds or damaged skin.

What should I do if I accidentally swallow the cream?

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

Can I use INK Kulture LIDO Cream during pregnancy?

The safety of lidocaine HCL cream during pregnancy has not been established, and it should only be used if the potential benefits justify the potential risks to the fetus.

What precautions should I take when using this cream?

You should avoid contact with eyes, and stop use and ask a doctor if the condition worsens, symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days.

How should I store INK Kulture LIDO Cream?

Store the cream at room temperature and do not use it if the seal is broken.

Packaging Info

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

Packaging configurations for Inkkulture Numbing.
Details

Drug Information (PDF)

This file contains official product information for Inkkulture 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 assess the necessity and safety of treatment in this age group before proceeding with any application.

Contraindications

There are no specific contraindications associated with this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed.

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 discontinue use and seek medical guidance.

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 Inkkulture Numbing (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Inkkulture Numbing.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area up to 3 to 4 times daily. For children under 2 years of age, the use of this medication is not recommended, and consultation with a physician is advised.

Geriatric Use

Elderly patients do not have specific geriatric use considerations, dosage adjustments, or safety concerns associated with the use of INKKULTURE NUMBING (lidocaine hcl cream) as indicated in the prescribing information. Therefore, healthcare providers may administer this medication to geriatric patients without the need for modifications based on age. However, standard clinical judgment should be exercised when treating elderly patients, taking into account their overall health status and any concomitant medications that may influence treatment outcomes.

Pregnancy

The safety of lidocaine HCL cream during pregnancy has not been established. The use of this medication is not recommended in pregnant patients unless the potential benefits justify the potential risks to the fetus. There may be risks associated with the use of lidocaine HCL cream in pregnant women, and it should be used with caution.

Dosage adjustments may be necessary for pregnant women, and it is advised that they consult with a healthcare provider prior to use. Special precautions should be taken, and pregnant women are encouraged to discuss the use of this product with their physician to ensure informed decision-making regarding its use during pregnancy.

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 and prepared for potential scenarios involving overdose.

Healthcare providers should be aware that the clinical presentation of an overdose may vary depending on the substance involved and the individual patient’s characteristics. Symptoms of overdose can range from mild to severe and may include altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of suspected overdosage, immediate medical evaluation is recommended. Healthcare professionals should assess the patient's vital signs and conduct a thorough clinical examination. Supportive care should be initiated as necessary, including airway management, oxygen supplementation, and intravenous fluids.

If the specific agent involved in the overdose is known, appropriate antidotes or treatments should be administered as per established guidelines. Continuous monitoring of the patient’s condition is crucial, and further interventions may be required based on the evolving clinical picture.

It is advisable for healthcare professionals to consult local poison control centers or toxicology experts for guidance on managing specific overdose cases. Documentation of the incident and any interventions performed is also critical for ongoing patient care and legal considerations.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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 effectiveness. Additionally, users must ensure that the seal remains intact; the product should not be used if the seal is broken, as this may compromise safety and efficacy. Proper handling and storage conditions are crucial for optimal product performance.

Additional Clinical Information

For patients aged 2 years and older, the medication should be applied to the affected area no more than 3 to 4 times daily. For children under 2 years of age, use is not recommended without consulting a physician. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Inkkulture 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 Inkkulture 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.

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.