Naturally Inspired Dry Eye Relief

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 associated with dryness of the eye. It is also indicated for the temporary relief of discomfort resulting from minor irritations of the eye or exposure to environmental factors such as wind and sun.

Additionally, this drug serves as a protectant against further irritation and is utilized to relieve dryness of the eye. It functions as a lubricant to prevent additional irritation and to alleviate symptoms of dryness.

Dosage and Administration

Healthcare professionals are advised to follow the outlined procedures for the administration of the medication.

Prior to administration, it is essential to wash hands thoroughly to maintain hygiene. The tamper-evident ring should be removed, followed by the removal of the cap from the bottle.

To administer the medication, the bottle should be tilted downward or upside down. The healthcare professional should then squeeze the bottle gently to instill 1 or 2 drops into the affected eye(s) as needed.

After the administration of the drops, the bottle should be tilted downward and shaken lightly to eliminate any residual drops that may remain on the tip. Finally, the cap must be securely replaced after use to ensure the integrity of the product.

Contraindications

Use of this product is contraindicated in individuals with a known allergy to any of its ingredients.

Additionally, the product should not be used if the solution has changed color or become cloudy, if the tamper-evident seal is broken or missing, or if the bottle is damaged. These conditions may indicate compromised product integrity or safety.

Warnings and Precautions

For external use only. To prevent contamination, it is imperative that the tip of the container not be touched to any surface. In rare instances, hypersensitivity reactions may occur, which can manifest as redness, burning, swelling, or itching.

Healthcare professionals should advise patients to discontinue use and seek medical attention if they experience any of the following: eye pain, changes in vision, or persistent redness or irritation of the eye. Additionally, if the condition worsens or does not improve within 72 hours, a consultation with a physician is recommended.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

In clinical use, the product is indicated for external use only. Patients should be advised that in rare instances, hypersensitivity reactions may occur, manifesting as redness, burning, swelling, and itching at the application site.

It is crucial that patients do not use the product if they have a known allergy to any of its ingredients. Should patients experience any of the following symptoms, they are advised to stop using the product and consult a healthcare professional: eye pain, changes in vision, or continued redness or irritation of the eye. Additionally, if the condition being treated 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 Naturally Inspired Dry Eye Relief (glycerin). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

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 available regarding the use of this product during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this product to pregnant patients and weigh the potential risks and benefits. Women of childbearing potential should be counseled on the importance of effective contraception during treatment and the need to inform their healthcare provider if they become pregnant or plan to become pregnant while using this product.

Lactation

There are no specific warnings or precautions regarding the use of this product by 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, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous evaluation and appropriate interventions should be implemented based on the clinical presentation and severity of symptoms.

In all cases of suspected overdosage, the involvement of poison control and emergency medical services is recommended to ensure optimal patient care and safety.

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

In rare cases, hypersensitivity reactions have been reported, including symptoms such as redness, burning, swelling, and itching. These events were identified through voluntary reports and surveillance programs.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact a Poison Control Center immediately. This guidance is crucial for ensuring patient safety and minimizing potential risks associated with accidental exposure.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers. It should be stored at a temperature range of 59-77°F to maintain its efficacy. Once opened, the product must not be used for more than 30 days. Additionally, it is essential to adhere to the expiration date indicated on the bottom of the box to ensure safety and effectiveness.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Naturally Inspired Dry Eye Relief, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)