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Mueller First Aid Antiseptic

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredients
  • Lidocaine Hydrochloride 2 g/100 mL
  • Benzalkonium Chloride 0.13 g/100 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2013
Label revision date
March 16, 2020
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Lidocaine Hydrochloride 2 g/100 mL
  • Benzalkonium Chloride 0.13 g/100 mL
Other brand names
Dosage form
Spray
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 2013
Label revision date
March 16, 2020
Manufacturer
Mueller Sports Medicine, Inc.
Registration number
part348
NDC root
52564-330
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

Germa Spray Plus is a product designed for specific uses, although the exact details of its applications are not provided. It is important to note that this product has been effective since June 16, 2013. While the specific mechanism of action is not detailed, it is intended to serve a particular purpose in addressing certain needs. If you have questions about how it may benefit you, consider consulting a healthcare professional for more information.

Uses

It seems that there are no specific uses or indications provided for this medication. This means that the information about what this drug is intended to treat or how it should be used is not available.

Additionally, there are no mentions of teratogenic effects (which are harmful effects on a developing fetus) or nonteratogenic effects (which do not affect fetal development). If you have any questions or need further information about this medication, it's best to consult with a healthcare professional.

Dosage and Administration

To use this medication effectively, please refer to the image labeled "Germa Spray Plus Label(3).jpg" for detailed dosage information. This image will provide you with the specific amounts you need to take or apply.

Unfortunately, the information provided does not include specific details about how to administer the medication, such as the method (for example, whether it should be sprayed, taken orally, etc.) or how often you should use it. It's important to follow the instructions in the image closely to ensure you are using the medication correctly. If you have any questions or need further clarification, consider reaching out to a healthcare professional for guidance.

What to Avoid

You can feel confident using this medication, as there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence mentioned. This means that, based on the information provided, there are no particular conditions or risks that would prevent you from taking this medication safely. Always remember to follow your healthcare provider's instructions and reach out to them if you have any questions or concerns about your treatment.

Side Effects

You may not experience any specific side effects from this medication, as no adverse reactions have been listed in the provided information. It's important to stay informed and consult your healthcare provider if you have any concerns or experience unusual symptoms while taking this medication.

Warnings and Precautions

It appears that there are no specific warnings, precautions, or instructions provided in the information available. However, it's always important to be aware of your health and to consult with your healthcare provider if you have any concerns about your medication.

If you experience any unusual symptoms or side effects, it's advisable to stop taking the medication and reach out to your doctor for guidance. Additionally, if you feel that you are having a medical emergency, seek immediate help from a healthcare professional. Always prioritize your health and safety by staying informed and proactive in your care.

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 feel unwell after taking the medication, 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 after taking medication.

Pregnancy Use

There is currently no information available about the use of Mueller First Aid Antiseptic during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product to ensure it is safe for you and your baby. Always prioritize open communication with your doctor regarding any medications or treatments you may consider during this time.

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

When it comes to using this medication in children, the information provided does not specifically address pediatric use. This means there are no recommended ages, dosage differences, or safety concerns outlined for children. As a parent or caregiver, it's important to consult with a healthcare professional for guidance on the appropriate use of this medication in younger patients, as they may have different needs compared to adults. Always prioritize your child's safety and well-being by seeking expert advice.

Geriatric Use

When it comes to using this medication in older adults, specific information about its safety and effectiveness is not available. This means that if you or a loved one is an older adult, it's especially important to consult with a healthcare provider before starting this medication. They can help assess any potential risks and determine the best approach for your individual health needs.

Always keep in mind that older adults may have different responses to medications, so close monitoring and communication with your healthcare team are essential.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. This is particularly true if you have reduced creatinine clearance (a measure of how well your kidneys are filtering waste). Regular monitoring of your kidney function is essential, so your healthcare provider will likely recommend routine renal function tests to keep track of how well your kidneys are working. Staying in close contact with your healthcare team will help ensure that your treatment is safe and effective.

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 apply, but you should always consult your healthcare provider for personalized advice. They can help monitor your liver function and determine the best approach for your treatment.

Make sure to keep your doctor informed about your liver health, as they may need to conduct regular tests to ensure your safety while using any medication. Your well-being is a priority, so don't hesitate to ask questions or express any concerns you may have.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use alongside other treatments or tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions and share any concerns you may have regarding your medications or tests.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Once you open the product, be sure to discard it after use to maintain safety and quality. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is Germa Spray Plus?

Germa Spray Plus is a medical product, but specific details about its general description are not provided.

What are the indications and usage for Germa Spray Plus?

No specific indications or usage details are provided for Germa Spray Plus.

Are there any teratogenic effects associated with Germa Spray Plus?

No teratogenic effects are mentioned for Germa Spray Plus.

What dosage information is available for Germa Spray Plus?

For detailed dosage information, refer to the image 'Germa Spray Plus Label(3).jpg'.

Are there any contraindications for using Germa Spray Plus?

There are no contraindications listed for Germa Spray Plus.

What should I do in case of an emergency while using Germa Spray Plus?

The text does not provide specific instructions for emergency medical help.

How should I store Germa Spray Plus?

Store Germa Spray Plus at room temperature, protect it from light, and do not freeze. Discard it after opening.

Is there any information regarding the use of Germa Spray Plus during pregnancy?

The text does not provide information regarding the use of Germa Spray Plus during pregnancy.

What precautions should be taken for patients with renal impairment?

Patients with renal impairment may need dosage adjustments and should be closely monitored, with regular renal function tests.

Are there any specific instructions for nursing mothers regarding Germa Spray Plus?

There are no specific warnings or recommendations for nursing mothers provided in the text.

Packaging Info

Below are the non-prescription pack sizes of Mueller First Aid Antiseptic (benzalkonium chloride, lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Mueller First Aid Antiseptic.
Details

Drug Information (PDF)

This file contains official product information for Mueller First Aid Antiseptic, 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 and is presented as a clear, colorless to pale yellow liquid. It contains the active ingredient Germa Spray Plus. The formulation includes several inactive ingredients, specifically water, glycerin, propylene glycol, and flavoring agents.

Uses and Indications

This drug is indicated for use in patients as determined by the prescribing healthcare professional. Currently, there are no specific indications or usage details provided.

There are no known teratogenic or nonteratogenic effects associated with this drug. Healthcare professionals should consider the absence of these effects when evaluating treatment options for their patients.

Dosage and Administration

Healthcare professionals are advised to refer to the image "Germa Spray Plus Label(3).jpg" for comprehensive dosage information. Specific details regarding the route, method, and frequency of administration are not provided in the text. It is essential to consult the label for accurate dosing ranges and administration techniques to ensure safe and effective use of the product.

Contraindications

There are no contraindications listed for the use of this product. It is important to evaluate each patient's individual circumstances and medical history when considering treatment options.

Warnings and Precautions

The absence of specific warnings, general precautions, laboratory tests, and instructions for emergency medical help or cessation of use limits the ability to provide detailed guidance. However, it is imperative for healthcare professionals to remain vigilant and exercise clinical judgment when prescribing or administering treatments.

Healthcare providers should ensure that they are familiar with the patient's medical history and current medications to mitigate potential risks. Regular monitoring of the patient's condition is essential, and any adverse reactions or unexpected changes in health status should prompt immediate evaluation and intervention.

In the absence of specific laboratory tests mentioned, it is advisable to consider routine assessments relevant to the treatment being administered, as well as any necessary follow-up tests to ensure patient safety and treatment efficacy.

In situations where patients exhibit concerning symptoms or adverse effects, healthcare professionals should be prepared to provide appropriate emergency medical assistance and advise patients on when to seek immediate care. Additionally, clear communication regarding the signs and symptoms that warrant discontinuation of treatment and consultation with a healthcare provider is crucial for patient safety.

Overall, maintaining a proactive approach to patient management and ensuring open lines of communication can significantly enhance treatment outcomes and minimize risks.

Side Effects

There are no specific adverse reactions or warnings associated with the use of this product as indicated in the provided information. No additional adverse reactions or important notes have been reported. Therefore, healthcare professionals should monitor patients for any unexpected effects during treatment, although no specific side effects have been documented in clinical trials or postmarketing experiences.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of Mueller First Aid Antiseptic (benzalkonium chloride, lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Mueller First Aid Antiseptic.
Details

Pediatric Use

Pediatric use has not been specifically addressed in the available data. There are no recommended age ranges, dosing differences, safety concerns, or special precautions for pediatric patients, including infants, children, and adolescents. Healthcare professionals should exercise caution when considering the use of this medication in the pediatric population due to the lack of specific information.

Geriatric Use

Geriatric patients may exhibit altered pharmacokinetics and pharmacodynamics, which can affect the safety and efficacy of treatment. However, specific geriatric use information is not provided in the prescribing information.

Healthcare providers should exercise caution when prescribing this medication to elderly patients, particularly those aged 65 and older. It is advisable to closely monitor these patients for any adverse effects and to consider potential dose adjustments based on individual health status and response to therapy.

Due to the lack of specific data regarding geriatric use, clinical judgment should guide treatment decisions in this population, taking into account the unique needs and characteristics of elderly patients.

Pregnancy

There is currently no information available regarding the use of Mueller First Aid Antiseptic during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals should exercise caution when considering the use of this product in pregnant patients due to the lack of data on potential fetal impacts. It is advisable to weigh the benefits against any unknown risks when prescribing this antiseptic to women of childbearing potential.

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 information is available.

Renal Impairment

Renal impairment may necessitate dosage adjustments for patients with reduced kidney function. It is essential that patients with reduced creatinine clearance are closely monitored to ensure safety and efficacy. Regular renal function tests should be performed in patients with kidney problems to assess their renal status and guide appropriate therapeutic decisions.

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 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 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 an overdose. Symptoms 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 initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of antidotes or specific treatments should be considered based on the substance involved and the clinical presentation. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

Documentation of the incident, including the amount and timing of the substance taken, is crucial for effective treatment 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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

Postmarketing experience has identified the following adverse reactions reported voluntarily or through surveillance programs: skin irritation, allergic reactions, and contact dermatitis. These events have been documented in the context of routine pharmacovigilance activities.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage to ensure safety.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Additionally, once opened, the product must be discarded to ensure safety and efficacy.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Mueller First Aid Antiseptic, 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 Mueller First Aid Antiseptic, 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.