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Regener-Eyes Ophthalmic Solution Lite Xl

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Active ingredient
Glycerin 4 mg/1 mL
Other brand names
Drug class
Non-Standardized Chemical Allergen
Dosage form
Solution/ Drops
Route
Ophthalmic
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2026
Label revision date
January 29, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Glycerin 4 mg/1 mL
Other brand names
Drug class
Non-Standardized Chemical Allergen
Dosage form
Solution/ Drops
Route
Ophthalmic
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 2026
Label revision date
January 29, 2026
Manufacturer
M & M PRODUCTS, L. L. C.
Registration number
M018
NDC root
87354-001
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

Regener-Eyes Ophthalmic Solution LITE XL is an eye lubricant designed to provide temporary relief from burning and irritation caused by dryness of the eye. It contains glycerin (0.4%), which helps to moisturize and protect the eyes, preventing further irritation and alleviating dryness.

This preservative-free solution can be used as needed to soothe your eyes and is particularly helpful if you experience discomfort due to environmental factors or prolonged screen time.

Uses

If you're experiencing burning or irritation due to dry eyes, this product can help provide temporary relief. It's designed to act as a lubricant, which not only alleviates dryness but also protects your eyes from further irritation.

Regener-Eyes® is specifically formulated to soothe discomfort caused by dry eyes, and it’s preservative-free, making it a gentle option for your eye care needs. You can use it whenever you feel dryness or irritation to keep your eyes comfortable.

Dosage and Administration

To use this medication, you will need to put 1 or 2 drops directly into the affected eye or eyes whenever necessary. This means you can apply the drops as often as you feel you need them to help relieve your symptoms. Make sure to follow any specific instructions provided by your healthcare provider for the best results.

What to Avoid

There are no specific contraindications, controlled substance classifications, or risks of abuse, misuse, or dependence associated with this medication. This means that, based on the available information, you can use it without concerns about these particular issues. However, always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

You should be aware that this product is for external use only. To prevent contamination, avoid touching the tip of the container to any surface and always replace the cap after use. If the solution changes color or becomes cloudy, do not use it.

If you experience eye pain, changes in vision, or ongoing redness or irritation of the eye, stop using the product and consult a doctor. If your condition worsens or does not improve within 72 hours, seek medical advice. Additionally, keep this product out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

It's important to use this product only on the outside of your body. To prevent contamination, avoid touching the tip of the container to any surface, and always replace the cap after use. If the solution changes color or becomes cloudy, do not use it. Keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center right away.

You should stop using the product and consult your doctor if you experience any eye pain, changes in your vision, or if you notice ongoing redness or irritation in your eyes. If these symptoms worsen or do not improve after 72 hours, it's essential to seek medical advice.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to seek medical help right away. You can do this by contacting a Poison Control Center or going to the nearest emergency room.

Signs of an overdose may include unusual symptoms, so it's crucial to be aware of how you or the affected person is feeling. If you notice anything concerning, don’t hesitate to get help immediately. Your safety is the top priority.

Pregnancy Use

There is currently no specific information available regarding the use of Regener-Eyes Ophthalmic Solution Lite XL 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 medication to ensure it is safe for you and your baby. Always prioritize open communication with your doctor about any medications you are considering during pregnancy.

Lactation Use

Currently, there is no specific information available about the use of Regener-Eyes Ophthalmic Solution Lite XL for nursing mothers or its effects during breastfeeding. This means that if you are breastfeeding, it’s important to consult with your healthcare provider before using this product. They can help you understand any potential risks and make the best decision for you and your baby. Always prioritize your health and your infant's well-being when considering any medication.

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 right away or contact a Poison Control Center for immediate assistance. Taking these precautions can help ensure your child's safety.

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 considering factors like kidney function and changes in cognition (thinking and memory) that can occur with age.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for determining the appropriate use of this medication based on individual health needs. Always ensure that any treatment plan is tailored to your specific situation.

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 is safe and effective for your specific condition. They can help you understand any necessary precautions or adjustments based on your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

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 any treatments you are using are safe and effective for you. Always feel free to ask questions and share your complete list of medications and tests to avoid any potential issues.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. This means keeping it in a place that is neither too hot nor too cold, typically between 68°F and 77°F (20°C to 25°C).

When handling the product, make sure to do so with clean hands and in a clean environment to maintain its safety and effectiveness. Always follow any specific instructions provided with the product for optimal use. If you have any questions about disposal or other safety measures, refer to the guidelines included with your product.

Additional Information

If you have any questions or need more information, you can reach out at (656) 225-2260. There are no further details available at this time.

FAQ

What is Regener-Eyes Ophthalmic Solution LITE XL used for?

Regener-Eyes is an eye lubricant used for the temporary relief of burning and irritation due to dryness of the eye.

How should I use Regener-Eyes?

You should instill 1 or 2 drops in the affected eye(s) as needed.

What are the warnings associated with Regener-Eyes?

Regener-Eyes is for external use only. Avoid touching the tip of the container to any surface, and replace the cap after use. If the solution changes color or becomes cloudy, do not use it.

What should I do if I experience eye pain or changes in vision while using Regener-Eyes?

Stop using Regener-Eyes and ask a doctor if you experience eye pain, changes in vision, continued redness, or irritation of the eye, or if your condition worsens or persists for more than 72 hours.

Is Regener-Eyes safe for children?

Keep Regener-Eyes out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

What should I do if I have questions about Regener-Eyes?

You can call (656) 225-2260 for any questions regarding Regener-Eyes.

How should I store Regener-Eyes?

Store Regener-Eyes at room temperature.

Packaging Info

Below are the non-prescription pack sizes of Regener-Eyes Ophthalmic Solution Lite Xl (glycerin ophthalmic solution). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Regener-Eyes Ophthalmic Solution Lite Xl.
Details

Drug Information (PDF)

This file contains official product information for Regener-Eyes Ophthalmic Solution Lite Xl, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The formulation contains Glycerin as the active ingredient at a concentration of 0.4%. Inactive ingredients include Sterile Water and Tonicity Solution Sodium Chloride.

Uses and Indications

This drug is indicated for the temporary relief of burning and irritation due to dryness of the eye. It serves as a lubricant to prevent further irritation and to alleviate dryness of the eye. Additionally, this product acts as a protectant against further irritation and is specifically formulated to provide temporary relief from symptoms associated with dry eyes.

Regener-Eyes® is preservative-free, making it suitable for frequent use without the risk of preservative-related irritation. There are no teratogenic or nonteratogenic effects associated with this product.

Dosage and Administration

Healthcare professionals are advised to instill 1 or 2 drops of the medication in the affected eye(s) as needed. The frequency of administration should be determined based on the clinical condition of the patient and the response to treatment. It is important to ensure that the drops are administered in a sterile manner to prevent contamination.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

External use only. To prevent contamination, it is imperative that the tip of the container does not come into contact with any surface. The cap should be securely replaced after each use. If the solution exhibits any changes in color or becomes cloudy, it must not be used.

Healthcare professionals should advise patients to discontinue use and seek medical attention if they experience any of the following symptoms: eye pain, changes in vision, persistent redness, or irritation of the eye. If these conditions worsen or do not improve within 72 hours, it is essential to consult a physician.

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

In summary, vigilance in monitoring for adverse effects and adherence to safety precautions is crucial for the safe use of this product.

Side Effects

Patients should be aware of the following warnings and precautions associated with the use of this product. It is intended for external use only. To prevent contamination, patients should avoid touching the tip of the container to any surface and ensure the cap is replaced after each use.

In the event that the solution changes color or becomes cloudy, it should not be used. Patients are advised to discontinue use and consult a healthcare professional if they experience any of the following symptoms: eye pain, changes in vision, persistent redness, or irritation of the eye. If these conditions worsen or do not improve within 72 hours, medical advice should be sought.

Additionally, this product should be kept out of reach of children. In the case of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

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 Regener-Eyes Ophthalmic Solution Lite Xl (glycerin ophthalmic solution). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Regener-Eyes Ophthalmic Solution Lite Xl.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

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

There is no specific information regarding the use of Regener-Eyes Ophthalmic Solution Lite XL during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in women who are pregnant or may become pregnant. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes in the absence of clinical data.

Lactation

There is no specific information regarding nursing mothers or lactation considerations provided in the drug insert for Regener-Eyes Ophthalmic Solution Lite XL. Therefore, the effects on breastfed infants and the excretion of the drug in human milk remain unknown. Healthcare professionals should exercise caution when prescribing this medication to lactating mothers.

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 lack of data when prescribing to this patient population.

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 event of an overdosage, it is imperative to seek immediate medical assistance. If the substance is ingested, healthcare professionals should be contacted without delay, or the individual should reach out to a Poison Control Center for guidance.

Prompt intervention is crucial to mitigate potential adverse effects associated with overdosage. Healthcare providers are advised to monitor the patient closely for any symptoms that may arise and to initiate appropriate management procedures based on the clinical presentation.

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 in the provided text.

Patient Counseling

Healthcare providers should encourage patients to reach out with any questions or concerns they may have regarding their treatment. Patients can contact the dedicated support line at (656) 225-2260 for assistance. It is important for healthcare providers to ensure that patients feel comfortable seeking clarification on any aspect of their care.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers assigned for identification. It is essential to store the product at room temperature to maintain its integrity and efficacy. Proper handling should be observed to ensure optimal conditions are met throughout the storage period.

Additional Clinical Information

Patients and clinicians may direct any questions regarding the medication to the provided contact number: (656) 225-2260.

Drug Information (PDF)

This file contains official product information for Regener-Eyes Ophthalmic Solution Lite Xl, 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 Regener-Eyes Ophthalmic Solution Lite Xl, 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.