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Aloe Ice Sunburn Relief

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Active ingredient
Lidocaine Hydrochloride 2 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2014
Label revision date
January 28, 2026
Active ingredient
Lidocaine Hydrochloride 2 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2014
Label revision date
January 28, 2026
Manufacturer
Aloe Care International, LLC
Registration number
M017
NDC root
61477-101

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

Aloe Ice is a topical product designed to provide temporary relief from pain associated with minor burns. It is formulated to soothe the skin and help alleviate discomfort, making it a helpful option for those experiencing minor burn injuries.

Uses

If you’re dealing with temporary pain from minor burns, this medication can help provide relief. It’s specifically designed to ease the discomfort associated with these types of injuries, allowing you to feel more comfortable as you heal.

Rest assured, this medication does not have any known teratogenic effects, meaning it does not cause harm to a developing fetus. This makes it a safer option for those who may be pregnant or planning to become pregnant.

Dosage and Administration

When using this medication, make sure to apply it generously to the area that is affected. This means you should cover the entire area with a sufficient amount of the product to ensure it works effectively. Remember, applying too little may not provide the relief you need, so don’t hesitate to use enough to fully coat the skin where you’re experiencing issues.

What to Avoid

It's important to be aware of specific instructions regarding your use of this medication. You should stop using it and consult a doctor if your condition worsens, persists for more than 7 days, or if it clears up and then returns.

Currently, there are no listed contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. Always prioritize your health and seek professional advice if you have any questions or concerns.

Side Effects

It's important to use this product only on the skin and not to swallow it. Be careful to avoid getting it in your eyes; if that happens, rinse your eyes thoroughly with water.

If your condition worsens or does not improve after 7 days, or if it clears up and then comes back, you should stop using the product and consult a doctor.

Warnings and Precautions

This product is for external use only, so please do not swallow it. Be careful to avoid getting it in your eyes; if that happens, rinse your eyes thoroughly with water right away.

If your condition worsens or does not improve after 7 days, or if it clears up and then comes back, stop using the product and consult your doctor for further advice. Your health and safety are important, so don’t hesitate to seek help if you have any concerns.

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, call your local emergency number or go to the nearest hospital. Always keep medications out of reach of children 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

While the provided information does not specify any particular guidelines or safety concerns regarding the use of this medication during pregnancy, it is always important to approach any medication with caution if you are pregnant or planning to become pregnant. You should consult your healthcare provider to discuss any potential risks and to ensure that you are making informed decisions about your health and the health of your baby.

Remember, your healthcare provider can offer personalized advice based on your specific situation, including any necessary precautions or alternative options that may be safer during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, you can feel reassured that there are no specific warnings or recommendations regarding nursing mothers or lactation in the information provided. This means that, based on the available data, there are no known risks associated with breastfeeding while using this medication. However, it's always a good idea to consult with your healthcare provider about any concerns you may have regarding your health and breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children. This precaution helps prevent accidental ingestion, which can be dangerous. Always store it in a safe place where children cannot access it, ensuring their safety at all times. If you have any concerns or questions about the medication, don't hesitate to reach out to your healthcare provider for guidance.

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. If you or a loved one is an older adult, it’s always wise to discuss any medications with a healthcare provider, especially since older individuals may have different health needs and responses to treatments.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health conditions and any other medications being taken. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

Renal Impairment

If you have kidney 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 usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

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 regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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, your healthcare provider can help ensure that your treatment plan is safe and effective, taking into account all the medications and tests you may be using. Always feel free to ask questions and share your complete health history to avoid any potential issues.

Storage and Handling

To ensure the best performance of your product, store it at a temperature between 20°C to 25°C (68°F to 77°F). It's important to protect it from light to maintain its effectiveness. When you're not using the tube, make sure to keep it tightly closed to prevent contamination. Remember to discard the product after opening to ensure safety and efficacy. Following these guidelines will help you use the product safely and effectively.

Additional Information

You will apply this medication topically, which means you will apply it directly to the skin. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences related to this medication.

FAQ

What is Aloe Ice used for?

Aloe Ice is used for the temporary relief of pain associated with minor burns.

Are there any teratogenic effects associated with Aloe Ice?

No teratogenic effects have been mentioned for Aloe Ice.

How should I apply Aloe Ice?

You should apply Aloe Ice generously to the affected area.

What should I do if my condition worsens or persists?

Stop use and ask a doctor if your condition worsens or persists for more than 7 days, or if it clears up and returns.

Are there any warnings I should be aware of?

Aloe Ice is for external use only, should not be swallowed, and you should avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

How should I store Aloe Ice?

Store Aloe Ice at 20°C to 25°C (68°F to 77°F), protect it from light, and keep the tube tightly closed when not in use.

Is Aloe Ice safe for children?

You should keep Aloe Ice out of reach of children.

Is there any specific information regarding its use during pregnancy or lactation?

The provided text does not mention any specific warnings or recommendations regarding the use of Aloe Ice during pregnancy or lactation.

Packaging Info

Below are the non-prescription pack sizes of Aloe Ice Sunburn Relief (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aloe Ice Sunburn Relief.
Details

Drug Information (PDF)

This file contains official product information for Aloe Ice Sunburn 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 associated with minor burns.

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

Dosage and Administration

Healthcare professionals are advised to apply the medication generously to the affected area. It is important to ensure that the application covers the entire area of concern to achieve optimal therapeutic effects.

Contraindications

There are no specific contraindications listed for this product. However, it is advised to discontinue use and consult a healthcare professional if the condition worsens, persists for more than 7 days, or resolves and then returns.

Warnings and Precautions

For external use only; this product is not intended for ingestion. It is imperative to avoid contact with the eyes. In the event of accidental eye contact, it is essential to rinse the eyes thoroughly with water to mitigate any potential irritation.

Healthcare professionals should advise patients to discontinue use and seek medical advice if the condition worsens or persists for more than 7 days, or if the condition appears to improve and then returns. Monitoring for these symptoms is crucial to ensure appropriate management and intervention.

Side Effects

Patients should be aware that this product is for external use only and must not be swallowed. Care should be taken to avoid contact with the eyes; in the event of contact, it is imperative to rinse the eyes thoroughly with water.

In clinical practice, patients are advised to stop using the product and consult a doctor if their condition worsens or persists for more than 7 days, or if the condition clears up and then returns. These precautions are essential to ensure the safety and well-being of individuals using the product.

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 Aloe Ice Sunburn Relief (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aloe Ice Sunburn Relief.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. It is essential to ensure that the medication is stored safely to prevent accidental ingestion or misuse by young children.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should be aware that the safety of this medication during pregnancy has not been specifically established. There are no available data regarding the potential risks or fetal impacts associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to weigh the potential benefits against any unknown risks. It is recommended that healthcare providers discuss the implications of medication use during pregnancy with their patients, ensuring informed decision-making.

Lactation

There are no specific warnings or recommendations regarding nursing mothers or lactation in the provided text. Therefore, healthcare professionals should consider the absence of data when advising lactating mothers about the use of this medication. It is advisable to monitor breastfed infants for any potential effects, although no specific concerns have been noted in the available information.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the lack of information necessitates careful clinical judgment and monitoring.

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

There is currently no specific information available regarding overdosage for this medication. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Continuous monitoring of vital signs and clinical status is essential to ensure patient safety.

Healthcare professionals should also consider consulting a poison control center or relevant toxicology resources for guidance on management strategies tailored to the specific circumstances of the overdosage event.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important for patients to understand that if their condition worsens or persists for more than 7 days, or if it clears up and then returns, they should stop using the medication and consult a doctor. This guidance is essential to ensure patient safety and effective management of their condition.

Storage and Handling

The product is supplied in a tube format, with specific storage and handling requirements to ensure its integrity and efficacy. It should be stored at a temperature range of 20°C to 25°C (68°F to 77°F) and must be protected from light exposure. To maintain the product's quality, the tube should be kept tightly closed when not in use. Additionally, it is important to discard the product after opening to prevent any potential degradation.

Additional Clinical Information

The route of administration for the product is topical. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Aloe Ice Sunburn 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 Aloe Ice Sunburn 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.

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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.