ADD CONDITION
First Aid Antiseptic
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This product has been discontinued
- Active ingredients
- Lidocaine Hydrochloride 25 mg/1 mL
- Benzalkonium Chloride 1.3 mg/1 mL
- Other brand names
- 2677 First Aid Burn Cream (by Prostat First Aid Llc)
- Afassco First Aid Burn Cream (by Afassco Inc.)
- Alocane Max (by Quest Products Llc)
- Alocane Max (by Quest Products Llc)
- Alocane Max (by Quest Products Llc)
- Alocane Plus (by Quest Products Llc)
- Alocane Plus (by Quest Products, Inc.)
- Alocane Plus (by Quest Products, Inc.)
- Antibacterial Lidocaine Wound Gel (by Aso Llc)
- Antibacterial Lidocaine Wound Gel (by Cvs Pharmacy)
- Antibacterial Lidocaine Wound Gel (by Walgreens)
- Antibacterial Lidocaine Wound Gel (by Water-Jel Technologies, Llc)
- Aosi Healthcare Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Aramark Burn Cream (by Western First Aid Safety Dba Aramark)
- Astonea Burn Cream (by Astonea Labs Private Limited)
- Burn (by Ningbo Tianbo First Aid Product Co. , Ltd.)
- Burn Cream (by Trifecta Pharmaceuticals Usa Llc)
- Burn First Aid (by Dynarex Corporation)
- Crane Safety Burn (by Crane Safety Llc)
- Cvs Health Antiseptic Wound Wash (by Cvs Pharmacy)
- Cvs Pain Relieving First Aid Antiseptic (by Cvs Pharmacy)
- Dg Health (by Dollar General Corporation)
- Dynarex Burn Cream (by Dynarex Corporation)
- First Aid Antiseptic (by Dollar General)
- First Aid Antiseptic (by Premier Value)
- First Aid Antiseptic (by Rite Aid)
- First Aid Antiseptic (by Walgreens)
- First Aid Burn (by Epic Medical Supply Corp)
- First Aid Burn (by Water-Jel Technologies)
- First Aid Burn Cream (by Davemed Healthcare Co. , Ltd)
- First Aid Burn Cream (by Front Line Safety)
- First Aid Burn Cream (by Prostat First Aid Llc)
- First Aid Burn Cream (by Prostat First Aid Llc)
- First Shield (by Unishield)
- Firstar Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Health and Beyond Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Hurricaine One (by Beutlich Pharmaceuticals Llc)
- Levigosp (by Topicare Management, Llc)
- Levigosp (by Topicare Management, Llc)
- Medi-First (by Orazen Inc)
- Medi-First (by Orazen Inc)
- Meijer Maximum Strength (by Meijer Distribution, Inc.)
- Mueller First Aid Antiseptic (by Mueller Sports Medicine, Inc.)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Pain Relieving Cleansing (by Target)
- Pain Relieving Cleansing Spary (by Trifecta Pharmaceuticals Usa, Llc.)
- Proheal Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Roosin Burn (by Roosin Medical Co. , Ltd)
- Safly Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Top Safety First Aid Burn Cream (by Top Safety Products Company Inc)
- View full label-group details →
- 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
- July 6, 2018
- Drug Information (PDF)
- Prescribing information, PDF file
- Active ingredients
- Lidocaine Hydrochloride 25 mg/1 mL
- Benzalkonium Chloride 1.3 mg/1 mL
- Other brand names
- 2677 First Aid Burn Cream (by Prostat First Aid Llc)
- Afassco First Aid Burn Cream (by Afassco Inc.)
- Alocane Max (by Quest Products Llc)
- Alocane Max (by Quest Products Llc)
- Alocane Max (by Quest Products Llc)
- Alocane Plus (by Quest Products Llc)
- Alocane Plus (by Quest Products, Inc.)
- Alocane Plus (by Quest Products, Inc.)
- Antibacterial Lidocaine Wound Gel (by Aso Llc)
- Antibacterial Lidocaine Wound Gel (by Cvs Pharmacy)
- Antibacterial Lidocaine Wound Gel (by Walgreens)
- Antibacterial Lidocaine Wound Gel (by Water-Jel Technologies, Llc)
- Aosi Healthcare Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Aramark Burn Cream (by Western First Aid Safety Dba Aramark)
- Astonea Burn Cream (by Astonea Labs Private Limited)
- Burn (by Ningbo Tianbo First Aid Product Co. , Ltd.)
- Burn Cream (by Trifecta Pharmaceuticals Usa Llc)
- Burn First Aid (by Dynarex Corporation)
- Crane Safety Burn (by Crane Safety Llc)
- Cvs Health Antiseptic Wound Wash (by Cvs Pharmacy)
- Cvs Pain Relieving First Aid Antiseptic (by Cvs Pharmacy)
- Dg Health (by Dollar General Corporation)
- Dynarex Burn Cream (by Dynarex Corporation)
- First Aid Antiseptic (by Dollar General)
- First Aid Antiseptic (by Premier Value)
- First Aid Antiseptic (by Rite Aid)
- First Aid Antiseptic (by Walgreens)
- First Aid Burn (by Epic Medical Supply Corp)
- First Aid Burn (by Water-Jel Technologies)
- First Aid Burn Cream (by Davemed Healthcare Co. , Ltd)
- First Aid Burn Cream (by Front Line Safety)
- First Aid Burn Cream (by Prostat First Aid Llc)
- First Aid Burn Cream (by Prostat First Aid Llc)
- First Shield (by Unishield)
- Firstar Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Health and Beyond Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Hurricaine One (by Beutlich Pharmaceuticals Llc)
- Levigosp (by Topicare Management, Llc)
- Levigosp (by Topicare Management, Llc)
- Medi-First (by Orazen Inc)
- Medi-First (by Orazen Inc)
- Meijer Maximum Strength (by Meijer Distribution, Inc.)
- Mueller First Aid Antiseptic (by Mueller Sports Medicine, Inc.)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Numbify Sanitize (by Ridge Properties)
- Pain Relieving Cleansing (by Target)
- Pain Relieving Cleansing Spary (by Trifecta Pharmaceuticals Usa, Llc.)
- Proheal Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Roosin Burn (by Roosin Medical Co. , Ltd)
- Safly Burn (by Nantong Health & Beyond Hygienic Products Inc.)
- Top Safety First Aid Burn Cream (by Top Safety Products Company Inc)
- View full label-group details →
- 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
- July 6, 2018
- Manufacturer
- Meijer
- Registration number
- part348
- NDC root
- 41250-805
- Drug Information (PDF)
- Prescribing information, PDF file
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
This medication is designed for first aid use to help prevent bacterial contamination or skin infections. It can provide temporary relief from pain and itching associated with minor cuts, scrapes, burns, sunburn, and skin irritations. If you experience any of these skin issues, this drug may be a helpful option for you.
Uses
You can use this product for first aid to help prevent bacterial contamination or skin infections. It is also effective for providing temporary relief from pain and itching caused by minor cuts, scrapes, burns, sunburn, and skin irritations. This means that if you have a small injury or irritation on your skin, this product can help soothe the discomfort and protect the area from potential infection.
Dosage and Administration
To use this medication, start by cleaning the affected area thoroughly. For adults and children aged 2 years and older, apply a small amount of the medication to the area you want to treat. You can do this 1 to 3 times a day, depending on your needs. If you prefer, you can cover the area with a sterile bandage, but make sure to let the medication dry first.
If you have a child under 2 years old, it's important to consult a physician (doctor) before using this medication. They can provide guidance on the best course of action for your child's specific situation.
What to Avoid
It's important to use this product safely to avoid any potential issues. You should not use it in or near your eyes, as this can cause irritation or harm. Additionally, avoid applying it over large areas of your body or in large quantities, as this may lead to unwanted effects. Lastly, do not apply it over raw surfaces or blistered areas, as this can exacerbate irritation or discomfort. Always follow these guidelines to ensure your safety and well-being.
Side Effects
When using this product, it's important to apply it only to the skin and avoid contact with your eyes. You should not use it over large areas of your body or on raw or blistered skin. If your condition worsens, if symptoms last more than seven days, or if they improve and then return within a few days, stop using the product and consult a doctor.
Keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately.
Warnings and Precautions
This product is for external use only, so please avoid using it on any internal areas. Before using it, consult your doctor if you have deep or puncture wounds, animal bites, or serious burns. While using the product, be careful not to apply it near your eyes, over large areas of your body, or on raw or blistered skin.
If your condition worsens, or if your symptoms last more than 7 days or return after clearing up, stop using the product and contact your doctor. In case of accidental swallowing, seek emergency medical help or contact a Poison Control Center immediately.
Overdose
If you or someone else has swallowed too much of this medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room.
Signs of an overdose can vary, but they may include unusual symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to reach out for help. Remember, acting quickly can make a significant difference in ensuring safety and health.
Pregnancy Use
If you are pregnant or planning to become pregnant, it's important to know that the provided drug insert for the first aid antiseptic containing benzalkonium (0.13%) and lidocaine (2.5%) does not include any specific warnings, precautions, or dosage changes related to pregnancy. This means that, based on the information available, there are no known risks associated with using this product during pregnancy.
However, as with any medication or treatment, it's always a good idea to consult with your healthcare provider before using it, to ensure it’s safe for your individual situation.
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 to your infant. This means that, based on current knowledge, you can use this product without concern for its effects on your milk production or your baby’s health.
Pediatric Use
If your child is under 2 years old, it's important to consult a physician (doctor) before using this medication. For children aged 2 years and older, you should first clean the affected area. Then, apply a small amount of the medication to the area 1 to 3 times a day. If needed, you can cover it with a sterile bandage, but make sure to let the area dry first before applying the bandage. Always follow these guidelines to ensure your child's safety and well-being.
Geriatric Use
When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider before starting the medication. 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
If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have renal impairment (kidney issues).
Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help monitor your kidney function and make any necessary adjustments to 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 should be used if you have hepatic impairment (liver issues).
Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.
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 with other drugs and tests. However, every individual is different, and your healthcare provider can help ensure that your treatment plan is safe and effective for you.
Always remember that discussing your full list of medications and any upcoming lab tests with your healthcare provider is crucial. This way, you can avoid any potential issues and receive the best care tailored to your needs.
Storage and Handling
To ensure the best performance and safety of your product, it's important to store it in a cool, dry place. Avoid exposing it to excessive heat, as this can compromise its effectiveness. When handling the product, make sure to do so with clean hands or gloves to maintain its integrity and prevent contamination.
If you have any specific components that come with the product, be sure to follow any additional instructions provided for their use and storage. Always dispose of any used materials according to local regulations to ensure safety and environmental responsibility.
Additional Information
No further information is available.
FAQ
What is the primary use of this drug?
This drug is indicated for first aid to help prevent bacterial contamination or skin infection.
What conditions does this drug provide relief for?
It provides temporary relief of pain and itching associated with minor cuts, scrapes, burns, sunburn, and skin irritations.
What should I do before applying the drug?
You should clean the affected area before applying a small amount of the drug 1-3 times daily.
Are there any contraindications for using this drug?
No specific contraindications are mentioned for this drug.
What precautions should I take when using this product?
Do not use in or near the eyes, apply over large areas, or on raw surfaces or blistered areas.
What should I do if my condition worsens?
Stop using the product and ask a doctor if your condition worsens or if symptoms persist for more than 7 days.
Is this drug safe for children?
For children under 2 years, consult a physician. For those 2 years and older, follow the application instructions.
Can I use this drug during pregnancy or while nursing?
There are no specific warnings or recommendations regarding use during pregnancy or nursing.
What should I do if the drug is swallowed?
If swallowed, get medical help or contact a Poison Control Center right away.
What are the storage instructions for this drug?
Avoid excessive heat when storing this product.
Packaging Info
Below are the non-prescription pack sizes of First Aid Antiseptic (benzalkonium 0.13%, lidocaine hcl 2.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Spray |
| ||
Product details Regulatory status — Discontinued NSDE (NDC Directory) reports this NDC as Not Marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
Drug Information (PDF)
This file contains official product information for First Aid Antiseptic, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.
Description
No relevant information is available for SPL code 34089-3.
Uses and Indications
This drug is indicated for first aid to help prevent bacterial contamination or skin infection. It provides temporary relief of pain and itching associated with minor cuts, scrapes, burns, sunburn, 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 affected area should be cleaned prior to application. A small amount of the medication should be applied to the area 1 to 3 times daily. If desired, the area may be covered with a sterile bandage after the medication has dried.
For children under 2 years of age, it is recommended to consult a physician before use.
Contraindications
Use is contraindicated in the following situations:
Application in or near the eyes is prohibited due to the potential for irritation or damage to ocular tissues.
Application over large areas of the body or in large quantities is contraindicated to prevent systemic absorption and potential adverse effects.
Application over raw surfaces or blistered areas is not recommended, as this may exacerbate irritation or lead to further complications.
Warnings and Precautions
For external use only.
Healthcare professionals should advise patients to consult a physician prior to use if they have deep or puncture wounds, animal bites, or serious burns. During the application of this product, it is imperative to avoid contact with the eyes and to refrain from applying it over large areas of the body or in excessive quantities. Additionally, the product should not be used on raw surfaces or blistered areas.
Patients must be instructed to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.
In the event of accidental ingestion, immediate medical assistance should be sought, or the patient should contact a Poison Control Center without delay.
Side Effects
Patients using this product should be aware that it is intended for external use only. It is crucial to avoid application in or near the eyes, over large areas of the body, or in large quantities. Additionally, the product should not be applied over raw surfaces or blistered areas.
In the event that the condition worsens, or if symptoms persist for more than 7 days, or clear up and then recur within a few days, patients are advised to stop use and consult a doctor.
To ensure safety, this product should be kept out of reach of children. If swallowed, it is imperative to seek medical assistance or contact a Poison Control Center immediately.
Drug Interactions
There are no specific drug interactions or laboratory test interactions identified in the available data. Therefore, no recommendations for dosage adjustments or monitoring are necessary at this time.
Packaging & NDC
Below are the non-prescription pack sizes of First Aid Antiseptic (benzalkonium 0.13%, lidocaine hcl 2.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Spray |
| ||
Product details Regulatory status — Discontinued NSDE (NDC Directory) reports this NDC as Not Marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
Pediatric Use
Pediatric patients under 2 years of age should consult a physician prior to use. For children aged 2 years and older, the affected area should be cleaned before application. A small amount of the product may be applied to the area 1 to 3 times daily, and it may be covered with a sterile bandage after allowing it to dry.
Geriatric Use
There is no specific information 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.
Pregnancy
The safety of FIRST AID ANTISEPTIC - benzalkonium 0.13%, lidocaine hcl 2.5% spray during pregnancy has not been established. There are no specific warnings, precautions, or dosage modifications regarding its use in pregnant patients mentioned in the prescribing information.
Healthcare professionals should consider the potential risks and benefits when prescribing this product to women of childbearing potential. As with any medication, it is advisable to use caution and to discuss the use of this antiseptic spray with pregnant patients, particularly in the context of their overall treatment plan and any other medications they may be using.
Lactation
There are no specific warnings or recommendations regarding the use of this product by nursing mothers. Additionally, there is no information provided about the potential for excretion in breast milk or any associated risks to breastfed infants during lactation.
Renal Impairment
Patients with renal impairment have not been specifically addressed in the drug insert text 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 there is no available data to guide dosing or monitoring in this population.
Hepatic Impairment
Patients with hepatic impairment have not been specifically studied in relation to 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 prescribing information.
Overdosage
In the event of an overdosage, immediate medical assistance is crucial. Healthcare professionals are advised to instruct patients or caregivers to seek medical help or contact a Poison Control Center without delay if the substance has been ingested.
Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. The specific symptoms of overdosage may vary depending on the substance involved; therefore, a thorough assessment and appropriate management strategies should be implemented based on clinical presentation and available guidelines.
It is imperative that healthcare providers remain vigilant and prepared to initiate supportive care and symptomatic treatment as necessary.
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.
Patient Counseling
Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, patients should seek medical help or contact a Poison Control Center immediately.
Patients should be instructed to discontinue use and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms clear up and then recur within a few days, patients should also stop use and seek medical advice.
It is important to inform patients that this product should not be used in or near the eyes. They should be cautioned against applying the product over large areas of the body or in large quantities. Furthermore, patients should avoid applying the product over raw surfaces or blistered areas.
Healthcare providers should recommend that patients consult a doctor before using this product if they have deep or puncture wounds, animal bites, or serious burns.
Storage and Handling
The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product in a controlled environment, avoiding exposure to excessive heat to maintain its integrity and efficacy. Proper handling procedures should be followed to ensure optimal storage conditions are met.
Additional Clinical Information
No further data are available.
Drug Information (PDF)
This file contains official product information for First Aid Antiseptic, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.