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Optase

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Active ingredient
Glycerin 2 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 2020
Label revision date
January 30, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Glycerin 2 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 2020
Label revision date
January 30, 2026
Manufacturer
Scope Health Inc
Registration number
M018
NDC root
72972-002
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

Optase Intense MDU is a product designed to relieve dryness of the eye. It acts as a lubricant and protectant, helping to prevent further irritation. This can be particularly helpful for individuals experiencing discomfort due to dry eyes, providing soothing relief and support for eye health.

Uses

If you're experiencing dryness in your eyes, this product can help relieve that discomfort. It works effectively as a lubricant, providing moisture to your eyes and acting as a protectant to prevent further irritation. This means you can use it to keep your eyes feeling comfortable and to shield them from additional dryness or irritation.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this product, making it a safe option for those concerned about such risks.

Dosage and Administration

Before using your eye drops, make sure to shake the bottle well. When you use it for the first time, remove the cap, hold the bottle upside down, and discard one drop to prepare it for use. To apply the drops, gently squeeze the bottle once to deliver one or two drops into the affected eye(s) as needed.

After you’ve used the drops, flick or shake the bottle vigorously downwards to ensure that no extra drops remain inside. Remember, you should not use more than 25 drops in a 24-hour period, and avoid delivering more than 25 drops in a row. This will help you use the medication safely and effectively.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. While there are no listed contraindications, controlled substance classifications, or risks of abuse or dependence, you should take care if the medication is swallowed. In such a case, seek medical help or contact a Poison Control Center immediately. Your safety is paramount, so please follow these guidelines closely.

Side Effects

If you experience any eye pain, changes in your vision, or ongoing redness or irritation of the eye, it's important to stop using the medication and consult your doctor. Additionally, if your symptoms worsen or do not improve within 72 hours, seek medical advice. These reactions can indicate a more serious issue that needs attention.

Warnings and Precautions

This product is for external use only, so please avoid using it in any other way. Once you open the bottle, make sure to use it within 3 months and before the expiration date. If the product changes color, becomes cloudy, or if the bottle or seal is damaged, do not use it. To prevent contamination, avoid touching the tip of the nozzle and always replace the cap tightly after use. Additionally, keep this product out of reach of children and do not use it if you are sensitive to any of its ingredients.

If you experience eye pain, changes in vision, or if redness or irritation continues for more than 72 hours, stop using the product and call 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 it’s crucial to act quickly if you suspect one has occurred. Always prioritize safety and don’t hesitate to reach out for professional assistance.

Pregnancy Use

The safety of this product during pregnancy has not been established, meaning that it’s unclear whether it could affect you or your developing baby. While there are no specific contraindications (conditions that would prevent use) listed for pregnant individuals, the potential risks to the fetus are also not detailed.

If you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before using this product. Currently, there are no dosage modifications or special precautions provided for pregnant individuals, so discussing your options with a medical professional is essential for your safety and that of your baby.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into your breast milk, so caution is advised. Since the effects on your nursing infant have not been thoroughly studied, be sure to keep an eye out for any unusual reactions in your baby. Your health and your baby's well-being are the top priorities, so staying informed and cautious is key.

Pediatric Use

It's important to keep this medication out of reach and sight of children to prevent accidental ingestion. If a child swallows the medication, seek medical help immediately or contact a Poison Control Center for assistance. Taking these precautions can help ensure your child's safety.

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 there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

It's always best to discuss your individual situation with your healthcare provider, who can offer personalized advice and ensure that any medications you take are safe and effective for you.

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 determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may want to conduct regular liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

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 provider can help ensure that your treatment plan is safe and effective for you. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

Storage and Handling

You can feel confident using this product, as there are no specific storage, handling, or disposal instructions provided. This means you can store it at room temperature and handle it like you would other similar items. Always ensure that you keep it in a clean environment to maintain its integrity. If you have any concerns about safety or usage, please consult your healthcare provider for guidance.

Additional Information

No further information is available.

FAQ

What is Optase Intense MDU used for?

Optase Intense MDU is used to relieve dryness of the eye and acts as a lubricant or protectant to prevent further irritation.

How should I use Optase Intense MDU?

Shake well before use, remove the cap, discard one drop, and gently squeeze the bottle to deliver one or two drops into the affected eye(s) as needed.

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

Stop using the product and consult your doctor if you feel eye pain, notice changes in vision, or if redness or irritation persists for more than 72 hours.

Is Optase Intense MDU safe to use during pregnancy?

The safety of Optase Intense MDU during pregnancy has not been established, and there are no specific contraindications listed.

Can nursing mothers use Optase Intense MDU?

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 I accidentally swallow Optase Intense MDU?

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

How long can I use Optase Intense MDU after opening?

Once opened, use Optase Intense MDU within 3 months and discard any unused product after this period.

Are there any specific warnings for using Optase Intense MDU?

Yes, it is for external use only, and you should not use it if the product changes color, becomes cloudy, or if the bottle or seal is damaged.

Packaging Info

Below are the non-prescription pack sizes of Optase (glycerin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Optase.
Details

Drug Information (PDF)

This file contains official product information for Optase, 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 relief of dryness of the eye. It serves as a lubricant or protectant to prevent further irritation.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The product should be shaken well before each use. Prior to the first application, the cap must be removed, and the bottle should be held upside down to discard one drop of the product. To administer the drop, the healthcare professional should gently squeeze and release the bottle once.

For treatment, one or two drops may be placed in the affected eye(s) as needed. After each use, it is essential to flick or shake the bottle vigorously downwards to ensure that no residual drop remains.

It is important to note that the maximum dosage should not exceed 25 drops within a 24-hour period, and no more than 25 drops should be delivered consecutively.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed.

Warnings and Precautions

For external use only. This product must be used within three months of opening and prior to the stated expiry date. Any unused product should be discarded after three months to ensure safety and efficacy. To prevent contamination, users should avoid touching, wiping, or cleaning the tip of the nozzle. It is essential to replace the cap tightly after each use.

The product should not be used if there are any changes in color or if it becomes cloudy. Additionally, it must not be used if the bottle or the tamper-evident seal is damaged, or if the applicator tip or bottle has been punctured, pierced, or otherwise tampered with. Individuals with known sensitivities to any ingredient in this product should refrain from use.

Patients are advised to discontinue use and consult a healthcare professional if they experience eye pain, changes in vision, or if redness or irritation of the eye persists or worsens beyond 72 hours.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

General precautions include keeping the product out of reach and sight of children to prevent accidental ingestion or misuse.

Side Effects

Patients should discontinue use and consult a healthcare professional if they experience any of the following: eye pain, changes in vision, persistent redness or irritation of the eye, or if their condition worsens or persists for more than 72 hours. These symptoms may indicate serious adverse reactions that require medical evaluation.

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 Optase (glycerin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Optase.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach and sight to prevent accidental ingestion. In the event of swallowing the medication, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

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 this product during pregnancy has not been established. There are no specific contraindications listed for use during pregnancy; however, the potential risks to the fetus are not explicitly mentioned in the prescribing information. No dosage modifications for pregnant individuals are provided, and no special precautions regarding use during pregnancy are detailed in the insert. Healthcare professionals should weigh the potential benefits against any unknown risks when considering this product for pregnant patients.

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; it is recommended to monitor for any adverse reactions in the infant.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data 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 the lack of information necessitates careful clinical judgment and monitoring of these patients.

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, immediate medical assistance is crucial. Healthcare professionals are advised to seek medical help or contact a Poison Control Center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved. It is essential for healthcare providers to assess the patient’s condition thoroughly and monitor for any adverse effects that may arise.

Management of overdosage should be guided by the clinical presentation and the specific characteristics of the substance. Supportive care and symptomatic treatment are often necessary. In cases of ingestion, activated charcoal may be considered if appropriate and within the recommended time frame. Continuous monitoring of vital signs and supportive measures should be implemented as needed.

Prompt recognition and intervention are key to minimizing potential complications associated with overdosage.

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 insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach and sight of children to prevent accidental ingestion. It is crucial to emphasize the importance of safety in the home environment, particularly for households with young children.

In the event that the medication is swallowed, healthcare providers should instruct patients to seek medical help immediately or contact a Poison Control Center. This prompt action is essential to ensure the safety and well-being of the patient.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. There are no specific storage, handling, or disposal instructions provided. Therefore, standard storage practices should be followed to ensure the integrity of the product. It is advisable to store the product in a cool, dry place, away from direct sunlight and moisture, to maintain its quality.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Optase, 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 Optase, 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.