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Foot Hangover

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This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2018
Label revision date
January 31, 2018
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Dosage form
Liquid
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 2018
Label revision date
January 31, 2018
Manufacturer
Ari Brands, Llc
Registration number
part348
NDC root
71436-0024
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

You can use this medication for the temporary relief of pain and itching caused by minor burns, sunburn, minor cuts, abrasions, insect bites, and minor skin irritations. It is designed to help soothe discomfort and promote healing for these common skin issues.

Uses

You can use this medication for the temporary relief of pain and itching caused by minor burns, sunburn, minor cuts, abrasions, insect bites, and other minor skin irritations. It’s designed to help soothe discomfort and promote healing in these common skin issues.

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 or your child is 2 years old or older, you can apply the medication directly to the affected area of the skin. You should do this up to 3 to 4 times a day, depending on your needs. Make sure to follow the instructions carefully to ensure the best results.

If your child is under 2 years old, it’s important to consult with a doctor before using this medication. They can provide guidance on the appropriate treatment for younger children. Always prioritize safety and follow professional advice when it comes to medication for little ones.

What to Avoid

It's important to keep this medication out of reach of children and pets to ensure their safety. If someone accidentally swallows it, seek medical help immediately or contact the Poison Control Center for guidance.

There are no specific contraindications, risks of abuse or misuse, or concerns about dependence associated with this medication. However, always use it responsibly and follow any additional instructions provided by your healthcare professional.

Side Effects

When using this product, it's important to be aware of some potential side effects and safety warnings. You should only use it externally and avoid contact with your eyes. The product is flammable, so refrain from using it while smoking or near any heat sources. It's also advised not to apply it in large amounts, especially on raw or blistered skin, or on large areas of the body. If your condition worsens, symptoms last longer than seven days, or if they clear up and return shortly after, stop using the product and consult a doctor. Additionally, if you are pregnant or breastfeeding, please consult a healthcare professional before use.

Warnings and Precautions

This product is for external use only, so be sure to avoid contact with your eyes. It is flammable, which means you should not use it while smoking or near any heat or flames. Use caution and do not apply it in large amounts, especially on raw surfaces, blistered areas, or on large areas of your body. Avoid using it on cut, irritated, or swollen skin, and do not use it for more than one week without consulting your doctor.

If your condition worsens, if symptoms last longer than 7 days, or if they clear up and then come back within a few days, stop using the product and contact your doctor. If you are pregnant or breastfeeding, please consult a healthcare professional before using this product. Keep it out of reach of children and pets, and if swallowed, seek medical help or contact the Poison Control Center immediately.

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.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

You can use this product on children aged 2 years and older by applying it externally up to 3 to 4 times a day. However, if your child is under 2 years old, it's important to consult a doctor before using it. This ensures that the product is safe and appropriate for your little one. Always follow the recommended guidelines to keep your child safe and healthy.

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 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 there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations for the medication do not change based on liver impairment. However, it’s always best to discuss your individual situation with your healthcare provider, as they can offer personalized advice and monitor your health closely.

Make sure to keep your doctor informed about your liver condition, as they may want to conduct regular liver function tests (which check how well your liver is working) to ensure your safety while using this medication.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool, dry place, avoiding temperatures above 120°F (49°C). This helps maintain the integrity of the contents, which are under pressure.

When using the product, always follow the instructions provided. It's important not to puncture or incinerate the container, as this could lead to dangerous situations. By handling the product carefully and adhering to these guidelines, you can ensure a safe experience.

Additional Information

You should apply this medication topically (on the skin) to the affected area. For adults and children aged 2 years and older, you can use it up to 3 to 4 times a day. If the patient is under 2 years old, it's important to consult a doctor before use.

FAQ

What is the drug used for?

The drug is used for the temporary relief of pain and itching due to minor burns, sunburn, minor cuts, abrasions, insect bites, and minor skin irritations.

How should I use this drug?

For adults and children 2 years and older, apply externally to the affected area up to 3 to 4 times a day. For children under 2 years, consult a doctor.

Are there any warnings I should be aware of?

Yes, it is for external use only, avoid contact with eyes, and do not use near heat or flame. Do not use in large quantities or for more than one week without consulting a physician.

What should I do if I swallow the drug?

If swallowed, get medical help or contact the Poison Control Center immediately.

Can I use this drug if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before use.

What should I do if my symptoms persist?

Stop use and ask a doctor if conditions worsen, symptoms persist for more than 7 days, or if they clear up and occur again within a few days.

Is there any specific information for elderly patients?

No specific information regarding geriatric use or safety concerns for elderly patients is provided.

What should I do if I have children under 2 years?

For children under 2 years, it is advised to ask a doctor before use.

Packaging Info

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

Packaging configurations for Foot Hangover.
Details

Drug Information (PDF)

This file contains official product information for Foot Hangover, 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 and itching associated with minor burns, sunburn, minor cuts, abrasions, 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 2 years and older, the recommended dosage is to apply the medication externally to the affected area up to 3 to 4 times daily. The application should be performed with clean hands, ensuring that the affected area is free from any contaminants prior to use.

For children under 2 years of age, it is advised to consult a physician before administration to determine the appropriate course of action.

Contraindications

Use is contraindicated in individuals who are unable to keep the product out of reach of children and pets. In the event of accidental ingestion, immediate medical assistance should be sought or the Poison Control Center contacted.

Warnings and Precautions

For external use only; direct contact with the eyes should be avoided to prevent irritation or injury. The product is flammable; therefore, it must not be used while smoking or in proximity to heat or open flames.

Caution is advised regarding the quantity of product applied. It should not be used in large amounts, particularly on raw surfaces, blistered areas, or extensive areas of the body. Application on cut, irritated, or swollen skin is contraindicated, and use should not exceed one week without prior consultation with a physician.

Healthcare professionals should instruct patients to discontinue use and seek medical advice if conditions worsen, if symptoms persist beyond 7 days, or if symptoms resolve and then recur within a few days.

For individuals who are pregnant or breastfeeding, it is essential to consult a healthcare professional before using this product to ensure safety for both the mother and child.

This product should be kept out of reach of children and pets. In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Side Effects

Patients should be aware of several important warnings associated with the use of this product. It is intended for external use only, and contact with the eyes should be avoided. The product is flammable; therefore, it should not be used while smoking or near heat or flame. Caution is advised against using large quantities, particularly over raw surfaces, blistered areas, or on large areas of the body. It should not be applied to cut, irritated, or swollen skin, nor should it be used for more than one week without consulting a physician.

In clinical practice, patients are advised to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than seven days, or if symptoms clear up and then recur within a few days. Additionally, pregnant or breastfeeding individuals should seek guidance from a health professional prior to use.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Foot Hangover.
Details

Pediatric Use

The product is indicated for external use in pediatric patients aged 2 years and older, with a recommended application frequency of up to 3 to 4 times daily. For infants and children under 2 years of age, it is advised to consult a healthcare professional prior to use.

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

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. It is important to assess the potential risks and benefits, as well as to consider any available data regarding fetal outcomes and lactation. Healthcare providers should evaluate the necessity of treatment in the context of the patient's overall health and circumstances.

Lactation

Lactating mothers are advised to consult a healthcare professional prior to using this medication. There is currently no available data regarding the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating individuals.

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 overall clinical context when prescribing to this patient population, as the lack of specific guidance necessitates careful evaluation of renal function and potential impacts on drug efficacy and safety.

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 when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks associated with 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 for SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children and pets to prevent accidental ingestion. It is important to emphasize the potential risks associated with swallowing the medication. Instruct patients that if the medication is swallowed, they should seek medical help or contact the Poison Control Center immediately. This guidance is crucial for ensuring the safety and well-being of both patients and their families.

Storage and Handling

The product is supplied in a pressurized container. It is essential to store the product at temperatures not exceeding 120°F to maintain its integrity and safety.

Healthcare professionals are advised to handle the product with care, adhering strictly to the usage instructions provided. Puncturing or incinerating the container is strictly prohibited to prevent potential hazards.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of up to 3 to 4 times daily for adults and children aged 2 years and older. For children under 2 years, it is advised to consult a physician before use.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Foot Hangover, 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 Foot Hangover, 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.