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Regener-Eyes Ophthalmic Solution Professional Strength Xl

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Active ingredient
Glycerin 5 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 5 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
87354-002
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 dryness, burning, and irritation in the eyes. It works by acting as a protective barrier, helping to soothe and prevent further irritation caused by dry eyes.

This preservative-free solution is specifically formulated to help you feel more comfortable by alleviating the symptoms associated with dry eyes, making it a helpful option for those experiencing discomfort.

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 important to note that each product is preservative-free, making it suitable for regular use. Whether you're looking to relieve existing dryness or prevent future irritation, this product can be a helpful option for your eye care needs.

Dosage and Administration

To use this eye medication, you should instill (put) 1 or 2 drops directly into the affected eye or eyes whenever you feel it's necessary. This means you can apply the drops as needed, depending on your symptoms. Make sure to follow any additional instructions provided by your healthcare provider to ensure 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 this medication without concerns about these particular issues.

However, it's always important to follow your healthcare provider's instructions and discuss any questions or concerns you may have about your treatment. If you experience any unusual symptoms or side effects, be sure to reach out to your healthcare professional for guidance.

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, stop using the product and consult a doctor, especially if your condition worsens or lasts more than 72 hours. Keep this product out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

It's important to use this medication 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.

You should stop using this product and contact your doctor if you experience any eye pain, changes in your vision, or if you notice ongoing redness or irritation in your eyes that lasts more than 72 hours. Keep this medication out of reach of children. If you accidentally swallow it, seek medical help or contact a Poison Control Center right away.

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 can vary, but they may include unusual symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to get 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 there is currently no information available about the use of Regener-Eyes Ophthalmic Solution during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions related to its use in pregnant individuals have not been established.

Before using this product, you should consult with your healthcare provider to discuss any potential risks and to ensure that you are making informed decisions about your eye care during pregnancy. Your health and the health of your baby are the top priority, so it's always best to seek professional advice.

Lactation Use

If you are breastfeeding, you can use Regener-Eyes Ophthalmic Solution without specific warnings or recommendations. Currently, there is no information available about whether this solution passes into breast milk or if it poses any risk to your nursing infant.

As always, it's a good idea to consult with your healthcare provider if you have any concerns about medications while breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If a child swallows it, seek medical help or contact a Poison Control Center right away. 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 wise to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so regular check-ins with your doctor can ensure safety and effectiveness.

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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help monitor your condition and make any necessary adjustments to your treatment plan.

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, every individual’s health situation is unique, and your healthcare provider can help ensure that your treatment is safe and effective. Always discuss any other medications or supplements you are using, as well as any lab tests you may need, to avoid potential issues.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. It's important to handle the container carefully; avoid touching the tip to any surfaces to prevent contamination. After each use, make sure to replace the cap securely. If you notice any changes in the solution's color or if it becomes cloudy, do not use it.

Keep the product out of reach of children. In case of accidental ingestion, seek medical assistance or contact a Poison Control Center right away. Remember to discard the product after opening to maintain safety.

Additional Information

If you have any questions about your medication, you can reach out for assistance at (656) 225-2260. It's important to stay informed and seek help whenever you need clarification or support regarding your treatment.

FAQ

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

Regener-Eyes is used for the temporary relief of burning and irritation due to dryness of the eye. It acts as a lubricant to prevent further irritation.

How should I use Regener-Eyes?

Instill 1 or 2 drops in the affected eye(s) as needed.

Are there any warnings I should be aware of?

Yes, it is for external use only. Avoid touching the tip of the container to any surface, and stop use if you experience eye pain or changes in vision.

Is Regener-Eyes safe to use during pregnancy?

There is no specific information regarding the use of Regener-Eyes during pregnancy in the provided drug insert.

Can nursing mothers use Regener-Eyes?

There are no specific warnings or recommendations regarding the use of Regener-Eyes in nursing mothers.

What should I do if I swallow Regener-Eyes?

If swallowed, get medical help or contact a Poison Control Center immediately.

How should I store Regener-Eyes?

Store at room temperature and keep out of reach of children. Discard after opening.

What should I do if the solution changes color or becomes cloudy?

Do not use the solution if it changes color or becomes cloudy.

Packaging Info

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

Packaging configurations for Regener-Eyes Ophthalmic Solution Professional Strength Xl.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the temporary relief of 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.

Each formulation is preservative-free, ensuring safety and compatibility for patients requiring relief from ocular dryness. There are no teratogenic or nonteratogenic effects associated with this drug.

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 not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence.

Warnings and Precautions

External use only is mandated for this product. To prevent contamination, it is crucial that the tip of the container does not come into contact with any surfaces. After each use, the cap should be securely replaced. Should the solution change color or become cloudy, the product 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 the condition worsens or does not improve within 72 hours, medical consultation is necessary.

It is imperative to keep this product out of the reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

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, patients should not use the product. If patients experience eye pain, changes in vision, or continued redness or irritation of the eye, they should stop using the product and consult a doctor. Additionally, if the condition worsens or persists for more than 72 hours, medical advice should be sought.

This product should be kept out of reach of children. In the case of accidental ingestion, patients are advised to seek medical help 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 Professional Strength Xl (glycerin ophthalmic solution). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Regener-Eyes Ophthalmic Solution Professional Strength Xl.
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 contact with a Poison Control Center is recommended.

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 therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is currently no information available regarding the use of Regener-Eyes Ophthalmic Solution during pregnancy. This includes a lack of data on safety concerns, dosage modifications, or any special precautions that should be taken when considering treatment in pregnant patients. Healthcare professionals should weigh the potential benefits against any unknown risks when prescribing this medication to women of childbearing potential. Given the absence of specific data, it is advisable to exercise caution and consider alternative therapies when appropriate.

Lactation

There are no specific warnings or recommendations regarding the use of Regener-Eyes Ophthalmic Solution in lactating mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

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 a container that must be stored at room temperature. To maintain the integrity of the solution, it is essential to avoid contamination; therefore, the tip of the container should not come into contact with any surfaces. After each use, the cap should be securely replaced to prevent exposure to contaminants.

In the event that the solution changes color or becomes cloudy, it should not be used. It is important to keep the product out of reach of children. If the product is accidentally swallowed, immediate medical assistance should be sought, or contact with a Poison Control Center is advised. Additionally, the product should be discarded after opening to ensure safety and efficacy.

Additional Clinical Information

Patients and clinicians are encouraged to reach out with any questions regarding the medication by contacting (656) 225-2260. No further information is available concerning laboratory tests, abuse potential, administration routes, methods, frequency, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Regener-Eyes Ophthalmic Solution Professional Strength 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 Professional Strength 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.