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Glycerin

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This product has been discontinued

Active ingredient
Glycerin 25 mg/5 mL
Other brand names
Dosage form
Solution/ Drops
Route
Ophthalmic
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
January 29, 2026
Active ingredient
Glycerin 25 mg/5 mL
Other brand names
Dosage form
Solution/ Drops
Route
Ophthalmic
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2025
Label revision date
January 29, 2026
Manufacturer
Regenerative Processing Plant, LLC
Registration number
M018
NDC root
82305-103

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If you are a consumer or patient please visit this version.

Drug Overview

This medication is designed to provide temporary relief from burning and irritation caused by dryness of the eye. It works as a lubricant to help soothe your eyes and prevent further irritation. Additionally, it acts as a protectant, offering relief from dryness and helping to maintain comfort throughout the day.

If you experience discomfort due to dry eyes, this product may be a helpful option to consider for alleviating those symptoms.

Uses

If you're experiencing burning or irritation due to dry eyes, this product can provide temporary relief. It acts as a lubricant, helping to soothe your eyes and prevent further irritation. Additionally, it serves as a protectant, offering comfort and relief from dryness. You can use it to keep your eyes feeling more comfortable throughout the day.

Dosage and Administration

To use this medication, you will need to put 1 or 2 drops directly into the affected eye or eyes. You can do this as needed, depending on your symptoms. Make sure to follow any specific instructions provided by your healthcare provider for the best results.

What to Avoid

It's important to keep this medication out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center right away. There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. Always use it responsibly and as directed.

Side Effects

When using this medication, it's important to remember that it 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.

You should stop using the product and consult a doctor if you experience any eye pain, changes in vision, or if you notice continued redness or irritation in your eye. Additionally, if your condition worsens or does not improve within 72 hours, seek medical advice.

Warnings and Precautions

This product is for external use only. To keep it safe and effective, avoid touching the tip of the container to any surface, and always replace the cap after use. If you notice that 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 vision, or if redness or irritation continues. If your condition worsens or does not improve within 72 hours, seek medical advice.

In case of accidental swallowing, it’s important to get emergency medical help right away or contact a Poison Control Center. Your safety is a priority, so please take these precautions seriously.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, call your local emergency number or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no specific information available about the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions have not been clearly outlined.

Given this lack of information, it is advisable to consult with your healthcare provider before using this medication. They can help you weigh the potential risks and benefits based on your individual circumstances. Always prioritize open communication with your doctor regarding any medications you may be considering during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult with your healthcare professional before using this product. There is a possibility that the ingredients may pass into your breast milk, so caution is advised. Since the effects on your nursing infant have not been thoroughly studied, it's essential to weigh the potential risks against the benefits of using this product.

Pediatric Use

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should seek medical help right away or contact a Poison Control Center for immediate assistance. Always be vigilant to ensure that medications are stored safely to prevent any accidental ingestion.

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 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

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 determine the best approach for managing your health, especially if you have concerns about your kidneys.

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 discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you. Always share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance and safety 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 integrity. Always follow any specific instructions provided with the product for safe use and disposal.

Additional Information

If you have any questions or need support regarding your medication, you can reach out to the patient counseling service at (800) 781-0818. They are available to provide you with the information you need.

Currently, there is no further information available.

FAQ

What is the purpose of this eye drop?

This eye drop is for the temporary relief of burning and irritation due to dryness of the eye. It acts as a lubricant and protectant to prevent further irritation.

How should I use this eye drop?

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

Are there any contraindications for this eye drop?

No contraindications are listed for this eye drop.

What should I do if I experience eye pain or changes in vision?

You should stop using the eye drop and ask a doctor if you experience eye pain, changes in vision, or if the condition worsens or persists for more than 72 hours.

Is this eye drop safe to use during pregnancy?

There is no specific information regarding the safety of this eye drop during pregnancy, so consult a healthcare professional before use.

Can nursing mothers use this eye drop?

Nursing mothers should consult a healthcare professional before using this product, as there is a potential for excretion in breast milk.

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

If the solution changes color or becomes cloudy, do not use it.

How should I store this eye drop?

You should store the eye drop at room temperature.

What should I do if I accidentally swallow the eye drop?

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

Is this eye drop suitable for children?

You should keep this eye drop out of reach of children.

Packaging Info

Below are the non-prescription pack sizes of Regener-Eyes. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Regener-Eyes.
Details

Drug Information (PDF)

This file contains official product information for Regener-Eyes, 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 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, it functions as a protectant against further irritation and to relieve dryness of the eye.

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

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Warnings and Precautions

External use of this product is strictly advised. To prevent contamination, healthcare professionals should instruct patients not to touch the tip of the container to any surface and to ensure the cap is replaced immediately after use.

In the event that the solution changes color or becomes cloudy, it is imperative that the product is not used, as this may indicate a loss of efficacy or safety.

Patients should be advised to discontinue use and consult a physician if they experience any of the following symptoms: eye pain, changes in vision, persistent redness, or irritation of the eye. Additionally, if the condition worsens or does not improve within 72 hours, medical advice should be sought.

In cases of accidental ingestion, immediate medical assistance should be obtained, or the patient should contact a Poison Control Center without delay.

Side Effects

Patients should be aware of the following warnings and recommendations regarding 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. If the solution changes color or becomes cloudy, it should not be used.

Patients are advised to stop using the product and consult a doctor if they experience any of the following: eye pain, changes in vision, continued redness, or irritation of the eye. Additionally, if the condition worsens or persists for more than 72 hours, medical advice should be sought.

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. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Regener-Eyes.
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 adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is no specific information 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. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in the absence of established safety profiles. Women of childbearing potential should be counseled on the importance of effective contraception while using this medication.

Lactation

Nursing mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk; therefore, caution is advised when administering to nursing mothers. The effects on the nursing infant are not well studied; thus, the risks versus benefits should be considered.

Renal Impairment

Patients with renal impairment may not have specific dosage adjustments, special monitoring, or safety considerations outlined in the prescribing information. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data necessitates careful clinical judgment. Regular monitoring of renal function is advisable to ensure patient safety and therapeutic efficacy.

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 absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may arise from an overdose. Common symptoms may include, but are not limited to, severe drowsiness, confusion, respiratory distress, or any other unusual clinical manifestations.

Management of an overdose should be tailored to the individual patient and may involve supportive care, including monitoring vital signs and providing symptomatic treatment as necessary. In severe cases, specific interventions may be required, such as the administration of activated charcoal if the patient presents within a suitable timeframe post-ingestion.

It is crucial for healthcare professionals to consult local poison control guidelines and the product's prescribing information for further recommendations on the management of overdose situations.

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

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 regarding their treatment. Patients can contact the dedicated support line at (800) 781-0818 for assistance. It is important for healthcare providers to ensure that patients feel comfortable seeking clarification on their medication, potential side effects, and any other related inquiries.

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. No special handling requirements are necessary beyond standard storage practices.

Additional Clinical Information

Patients and clinicians can contact the provided helpline at (800) 781-0818 for any inquiries or counseling related to the medication. No further data are available.

Drug Information (PDF)

This file contains official product information for Regener-Eyes, 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, 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.