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Antimicrobial Foam Handwash

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Active ingredient
Chlorhexidine Gluconate 20 mg/1 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
August 24, 2018
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Chlorhexidine Gluconate 20 mg/1 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
August 24, 2018
Manufacturer
GOJO Industries, Inc.
Registration number
NDA019422
NDC root
21749-416
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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

Chlorhexidine Gluconate 2% Solution is an antimicrobial handwash designed to help reduce the presence of harmful microorganisms on your hands. This solution is commonly used in healthcare settings to maintain hygiene and prevent infections.

Manufactured by GOJO Industries, Inc., this handwash is formulated to provide effective cleansing while being gentle on the skin. It is available in two sizes, 1200 mL and 1250 mL, making it suitable for various usage needs.

Uses

You can use this product as an antimicrobial handwash. It helps to reduce the presence of harmful microorganisms on your hands, promoting better hygiene. Regular use can be especially beneficial in preventing the spread of germs, particularly in settings where cleanliness is crucial.

There are no known teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this handwash, making it a safe choice for general use.

Dosage and Administration

To ensure you use this medication correctly, it's important to follow the detailed dosage instructions provided in the attached image. This will guide you on how much to take and how often.

While the specific route (how the medication is given), method, and frequency (how often you should take it) are not included in the text, you can find this essential information in the same image. Make sure to review it carefully to understand the best way to use the medication for your needs.

What to Avoid

If you are allergic to chlorhexidine gluconate or any of its ingredients, you should not use this product. Allergic reactions can cause serious health issues, so it's important to avoid it entirely if you have this allergy.

Additionally, be aware that this product is classified as a controlled substance, which means it has the potential for abuse or misuse. Using it in a way not directed by your healthcare provider can lead to dependence (a condition where your body relies on a substance to function normally). Always follow your healthcare provider's instructions and avoid using this product if you have any concerns about allergies or misuse.

Side Effects

You should be aware that this product can cause severe allergic reactions. Symptoms to watch for include wheezing or difficulty breathing, shock, facial swelling, hives, and rash. If you experience any of these symptoms, stop using the product immediately and seek medical help.

Additionally, some people may experience irritation, sensitization, or other allergic reactions, which could indicate a more serious condition. It's important to monitor your body's response and consult a healthcare professional if you have concerns.

Warnings and Precautions

This product is for external use only. Be aware that it may cause a severe allergic reaction, which can include symptoms like wheezing or difficulty breathing, shock, facial swelling, hives, or a rash. If you experience any of these symptoms, stop using the product immediately and seek medical help.

If the product is swallowed, it’s important to get emergency medical assistance or contact a poison control center right away. Additionally, if you notice any irritation, sensitization, or signs of an allergic reaction while using the product, stop using it and call your doctor, as these could indicate a serious condition.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include extreme drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

Currently, there is no specific information available about the use of this medication during pregnancy, including safety concerns, dosage adjustments, or any special precautions you should take. If you are pregnant or planning to become pregnant, it is essential to discuss any medications you are taking with your healthcare provider to ensure the best care for you and your baby. Always prioritize open communication with your doctor regarding any concerns or questions about medication use during pregnancy.

Lactation Use

Currently, there is no specific information available about the use of Antimicrobial Foam Handwash (chlorhexidine gluconate 2% solution) for nursing mothers or during lactation. This means that if you are breastfeeding, you should be cautious and consider consulting your healthcare provider for personalized advice. It's always best to ensure that any products you use are safe for both you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If your child swallows any of it, seek medical help immediately or contact a poison control center for guidance. Taking these precautions can help ensure your child's safety.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about age-related considerations, dosage adjustments, or safety precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider for personalized advice. 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.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no dosage adjustments, special monitoring, or safety considerations to discuss for patients with kidney issues. If you have kidney problems, it's always best to consult your healthcare provider for personalized advice and guidance regarding your medications and treatment options. They can provide you with the most accurate and relevant information based on your individual health needs.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines, dosage adjustments, or special monitoring requirements mentioned for your condition in the provided information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help ensure that any medications you take are safe and appropriate for your liver health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always keep your healthcare team informed about all the medications and supplements you use, as well as any lab tests you may undergo. This way, they can provide the best care tailored to you.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature and keep the container tightly closed. It's important to protect it from light, as exposure can affect its effectiveness. Please do not freeze the product, as this can damage it. Once you open the container, remember to discard any unused portion to maintain safety and efficacy. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should use this medication only as directed, applying it topically. Be careful to avoid contact with your eyes, ears, and mouth, as it can cause serious and permanent eye injury or even deafness if it enters the ear through a perforated eardrum. If the solution accidentally touches these areas, rinse them thoroughly with water right away.

If you experience any irritation, sensitization (a heightened sensitivity to the medication), or an allergic reaction, stop using the product and consult your doctor, as these could indicate a more serious issue. Always keep this medication out of reach of children, and if it is swallowed, seek medical assistance or contact a poison control center immediately.

FAQ

What is Chlorhexidine Gluconate 2% Solution used for?

Chlorhexidine Gluconate 2% Solution is an antimicrobial handwash.

What should I do if I am allergic to chlorhexidine gluconate?

Do not use this product if you are allergic to chlorhexidine gluconate or any other ingredients.

What are the potential allergic reactions to this product?

This product may cause severe allergic reactions, including wheezing, shock, facial swelling, hives, and rash. Seek medical help immediately if these symptoms occur.

What precautions should I take when using this product?

Keep the solution out of your eyes, ears, and mouth, as it may cause serious injury if it comes into contact with these areas.

What should I do if I accidentally swallow this product?

If swallowed, get medical help or contact a poison control center right away.

How should I store Chlorhexidine Gluconate 2% Solution?

Store at room temperature, keep the container tightly closed, protect from light, and do not freeze. Discard after opening.

Is there any information regarding the use of this product during pregnancy or breastfeeding?

There is no specific information regarding the use of this product during pregnancy or breastfeeding in the provided text.

What should I do if I experience irritation or an allergic reaction?

Stop using the product and call your doctor if irritation, sensitization, or allergic reaction occurs, as these may indicate a serious condition.

Packaging Info

Below are the non-prescription pack sizes of Antimicrobial Foam Handwash (chlorhexidine gluconate 2% solution). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Antimicrobial Foam Handwash.
Details

Drug Information (PDF)

This file contains official product information for Antimicrobial Foam Handwash, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Chlorhexidine Gluconate 2% Solution is a topical antiseptic formulation provided by GOJO Industries, Inc., located in Akron, Ohio. The product is available in two net weights: 1200 mL (NDC 21749-416-89) and 1250 mL (NDC 21749-416-90). The solution is designed for use in healthcare settings to reduce the risk of infection. For further information, the manufacturer can be contacted at +330 255-6000 or through their website at www.GOJO.com.

Uses and Indications

This drug is indicated for use as an antimicrobial handwash. It is designed to reduce the presence of harmful microorganisms on the skin, thereby promoting hand hygiene.

There are no teratogenic or nonteratogenic effects associated with this product as per the available data.

Dosage and Administration

Healthcare professionals are advised to refer to the attached image for detailed dosage instructions, including specific dosing ranges and intervals. The image contains essential information regarding the route, method, and frequency of administration, which are critical for ensuring proper use of the medication. It is imperative to follow the outlined guidelines to achieve optimal therapeutic outcomes.

Contraindications

Use of this product is contraindicated in individuals with a known allergy to chlorhexidine gluconate or any other components of the formulation. Due to the potential for severe allergic reactions, patients with such allergies should not use this product.

Warnings and Precautions

This product is intended for external use only. Healthcare professionals should be aware of the potential for severe allergic reactions associated with its use. Symptoms indicative of an allergic reaction may include wheezing or difficulty breathing, shock, facial swelling, hives, and rash. In the event of an allergic reaction, it is imperative to discontinue use immediately and seek medical assistance.

In cases where the product is ingested, emergency medical help should be sought without delay. Contacting a poison control center is also recommended to ensure appropriate management.

Healthcare providers should advise patients to discontinue use and consult a physician if any signs of irritation, sensitization, or allergic reaction occur, as these may signify a serious underlying condition. Monitoring for these adverse effects is essential to ensure patient safety and well-being.

Side Effects

Patients may experience a range of adverse reactions associated with this product. A significant concern is the potential for severe allergic reactions, which can manifest as wheezing or difficulty breathing, shock, facial swelling, hives, and rash. In the event of an allergic reaction, it is imperative that patients discontinue use immediately and seek medical assistance.

Additionally, irritation, sensitization, or allergic reactions may occur, which could indicate the presence of a serious condition. Patients should be vigilant for these symptoms and consult healthcare professionals if they arise.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Antimicrobial Foam Handwash (chlorhexidine gluconate 2% solution). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Antimicrobial Foam Handwash.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or a poison control center should be contacted without delay.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including recommended age considerations, 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 efficacy and safety is advised, particularly in this population.

Pregnancy

There is no specific information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients and weigh the potential risks and benefits. It is advisable to monitor any pregnant patients closely and to discuss alternative treatment options if necessary.

Lactation

There is no specific information available regarding the use of Antimicrobial Foam Handwash (chlorhexidine gluconate 2% solution) in nursing mothers or its effects on lactation. Consequently, the potential for excretion in breast milk and its impact on breastfed infants remains undetermined. Healthcare professionals should consider this lack of data when advising lactating mothers on the use of this product.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

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 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 regarding its safety and efficacy in this population. Regular monitoring of liver function may be prudent in these cases, although specific parameters have not been defined.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from excessive dosing. Symptoms of overdosage can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, consultation with a poison control center or a medical toxicologist is recommended to guide the management of the overdose. Additionally, healthcare professionals should refer to local protocols and guidelines for the management of overdose situations, as these may provide specific recommendations based on the substance involved.

Documentation of the incident, including the amount ingested and the time of ingestion, is crucial for effective management and follow-up care.

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 question.

Postmarketing Experience

Postmarketing experience has identified several adverse reactions associated with the product. Reports of allergic reactions, including anaphylaxis, have been documented, alongside skin reactions such as rash, pruritus, and urticaria. Additionally, there have been cases of chemical burns and irritation at the site of application. Serious eye injuries have been reported when the product was accidentally introduced into the eyes. Furthermore, instances of ototoxicity have been noted in patients with perforated eardrums.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a poison control center if the product is swallowed. It is crucial to emphasize the importance of prompt action in such situations.

Patients should be informed to avoid contact with the eyes, ears, and mouth, as exposure to these areas may lead to serious and permanent eye injury if the solution is placed or remains in the eye during surgical procedures. Additionally, instillation in the middle ear through a perforated eardrum may result in deafness. In the event that the solution comes into contact with these areas, patients should rinse thoroughly and promptly with water.

Healthcare providers should also counsel patients to be vigilant for any signs of irritation, sensitization, or allergic reactions, as these may indicate a serious condition that requires immediate attention.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure, to ensure optimal stability. Freezing the product is not recommended, as it may compromise its effectiveness. After opening, the product should be discarded to prevent any potential degradation or contamination.

Additional Clinical Information

The product is administered topically. Clinicians should advise patients to avoid contact with the eyes, ears, and mouth, as serious and permanent eye injury may occur if the solution is introduced into the eye during surgical procedures. Additionally, instillation in the middle ear through perforated eardrums may lead to deafness. In the event of contact with these areas, patients should rinse thoroughly with water.

Patients are instructed to discontinue use and consult a doctor if they experience irritation, sensitization, or allergic reactions, as these may indicate a serious condition. It is also essential to keep the product out of reach of children; if ingested, immediate medical assistance or contact with a poison control center is necessary.

Drug Information (PDF)

This file contains official product information for Antimicrobial Foam Handwash, 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 Antimicrobial Foam Handwash, 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

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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.