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Refresh Digital
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- Active ingredients
- Glycerin 10 mg/1 mL
- Carboxymethylcellulose Sodium 5 mg/1 mL
- Polysorbate 80 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 2020
- Label revision date
- November 28, 2022
- Drug Information (PDF)
- Prescribing information, PDF file
- Active ingredients
- Glycerin 10 mg/1 mL
- Carboxymethylcellulose Sodium 5 mg/1 mL
- Polysorbate 80 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 2020
- Label revision date
- November 28, 2022
- Manufacturer
- Allergan, Inc.
- Registration number
- M018
- NDC root
- 0023-6952
- Drug Information (PDF)
- Prescribing information, PDF file
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
Refresh® Digital Lubricant Eye Drops are designed to provide fast-acting relief for dry eyes. They contain HydroCell™, which helps soothe the burning, irritation, and discomfort that can occur due to dryness or exposure to environmental factors like wind or sun. These eye drops can also act as a protectant against further irritation, making them a helpful option for anyone experiencing eye dryness.
Uses
If you're experiencing burning, irritation, or discomfort in your eyes due to dryness or exposure to wind or sun, this product can provide temporary relief. It works by soothing your eyes and helping to alleviate those uncomfortable sensations.
Additionally, it may serve as a protective barrier against further irritation, ensuring your eyes stay comfortable in challenging conditions. You can use it to help maintain eye comfort throughout your day.
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
It's important to be aware of certain situations when using this medication. You should stop using it and consult your doctor if you experience any eye pain, changes in your vision, ongoing redness or irritation of the eye, or if your condition worsens or lasts longer than 72 hours.
Currently, there are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always prioritize your health and safety by following these guidelines closely.
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 you notice any changes in the color of the solution, do not use it.
It's important to stop using the product and consult a doctor if you experience eye pain, changes in vision, or if you notice continued redness or irritation of the eye. 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
This product is for external use only, so please avoid applying it to any internal areas. To keep the solution clean, do not touch the tip of the container to any surface, and always replace the cap after use. If you notice any change in the color of the solution, do not use it.
You should stop using this product and contact your doctor if you experience eye pain, changes in your vision, ongoing redness or irritation of the eye, or if your condition worsens or does not improve after 72 hours. Additionally, keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately.
Overdose
If you or someone else has swallowed too much of a 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. Acting quickly can make a significant difference in the outcome.
Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose has occurred.
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. Currently, there are no specific contraindications (situations where the product should not be used) listed for pregnant individuals, and no information is available about potential risks to the fetus. Additionally, there are no recommended dosage modifications or special precautions for pregnant individuals.
If you are pregnant or planning to become pregnant, it’s important to discuss any medications or products you are considering with your healthcare provider to ensure they are safe for you and your baby.
Lactation Use
If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.
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 immediately or contact a Poison Control Center for guidance. 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 considering this medication, it’s important to consult with a healthcare provider. 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 feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.
Storage and Handling
To ensure the safety and effectiveness of your product, make sure to use it only if the tape seals on the top and bottom flaps are intact. Always check the expiration date marked on the container and use the product before that date. Once opened, remember to discard it 90 days later to maintain safety.
For proper storage, keep the product in a cool, dry place at a temperature between 59°F and 77°F (15°C and 25°C). It's also important to retain the carton for future reference, as it may contain useful information. Following these guidelines will help you use the product safely and effectively.
Additional Information
No further information is available.
FAQ
What is Refresh® Digital Lubricant Eye Drops used for?
Refresh® Digital Lubricant Eye Drops are used for the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun.
How should I use Refresh® Digital Lubricant Eye Drops?
You should instill 1 or 2 drops in the affected eye(s) as needed.
Are there any contraindications for using this product?
There are no specific contraindications listed for Refresh® Digital Lubricant Eye Drops.
What should I do if I experience eye pain or changes in vision?
You should stop using the drops and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.
Is Refresh® Digital Lubricant Eye Drops safe to use during pregnancy?
The safety of this product during pregnancy has not been established, and there are no specific contraindications listed.
What precautions should I take when using Refresh® Digital Lubricant Eye Drops?
For external use only, avoid touching the tip of the container to any surface, and do not use if the solution changes color.
How should I store Refresh® Digital Lubricant Eye Drops?
Store the drops at 59°-77°F (15°-25°C) and discard them 90 days after opening.
What should I do if the drops are swallowed?
If swallowed, get medical help or contact a Poison Control Center right away.
Packaging Info
Below are the non-prescription pack sizes of Refresh Digital (carboxymethylcellulose sodium, glycerin, polysorbate 80). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Solution/ Drops |
| ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
| Solution/ Drops |
| ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
Drug Information (PDF)
This file contains official product information for Refresh Digital, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.
Description
No description information is available for the drug.
Uses and Indications
This drug is indicated for the temporary relief of burning, irritation, and discomfort associated with dryness of the eye or exposure to wind or sun. It may also be utilized as a protectant against further irritation.
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 proper technique during administration to maximize efficacy and minimize contamination.
Contraindications
Use is contraindicated in patients who experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours. In such cases, it is advised to discontinue use and consult a healthcare professional.
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. The cap should be securely replaced after each use. If the solution exhibits any change in color, 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, or if the condition worsens or does not improve within 72 hours.
It is essential 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 should be made without delay.
Side Effects
Patients using this product should be aware of several important warnings and potential adverse reactions. The product is intended for external use only. To prevent contamination, patients are advised not to touch the tip of the container to any surface and to replace the cap after each use.
In the event that the solution changes color, it should not be used. Patients are instructed 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, or if the condition worsens or persists for more than 72 hours.
Additionally, this product should be kept out of reach of children. If swallowed, it is crucial 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 Refresh Digital (carboxymethylcellulose sodium, glycerin, polysorbate 80). Columns show Packaging, Formulation Type, and Active Ingredient Strength.
Details | ||||
|---|---|---|---|---|
| Solution/ Drops |
| ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
| Solution/ Drops |
| ||
Product details Regulatory status — Marketed All current FDA data sets list this NDC as actively marketed. FDA record dates for this NDC:
Active ingredients
Inactive ingredients
| ||||
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 the Poison Control Center should be contacted without delay.
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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.
Pregnancy
The safety of this product during pregnancy has not been established. There are no specific contraindications listed for use during pregnancy, and no information is provided regarding potential risks to the fetus. Additionally, no dosage modifications are mentioned for pregnant individuals, and no special precautions regarding use during pregnancy are specified. Healthcare professionals should consider the lack of established safety data when prescribing this product to pregnant patients.
Lactation
There are no specific warnings or recommendations regarding the use of this product in nursing 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 clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.
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.
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 provided in the insert.
Patient Counseling
Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. In the event that the medication is swallowed, patients should be instructed to seek medical help or contact a Poison Control Center immediately.
Additionally, patients should be informed to discontinue use and consult a doctor if they experience any of the following symptoms: eye pain, changes in vision, persistent redness or irritation of the eye, or if their condition worsens or does not improve after 72 hours. It is important for healthcare providers to emphasize these points to ensure patient safety and effective use of the medication.
Storage and Handling
The product is supplied in a secure carton, which should be retained for future reference. It is essential to ensure that the tape seals on the top and bottom flaps are intact before use. The product must be utilized before the expiration date indicated on the container. Once opened, the product should be discarded 90 days after opening to ensure safety and efficacy.
For optimal storage conditions, the product should be maintained at a temperature range of 59°-77°F (15°-25°C). Proper handling and adherence to these storage guidelines are crucial for preserving the integrity of the product.
Additional Clinical Information
No further data are available.
Drug Information (PDF)
This file contains official product information for Refresh Digital, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.