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| Product NDC Code | 71205-084 | ||||
|---|---|---|---|---|---|
| Drug Name | Gnp lubricating relief |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | OPHTHALMIC | ||||
| Dosage Form | SOLUTION/ DROPS | ||||
| RxCUI drug identifier | 1188426 | ||||
| Application Number | part349 | ||||
| Labeler Name | Proficient Rx LP | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Purpose Carboxymethylcellulose Sodium 0.5%...........Eye lubricant
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.Distributed by AmerisourceBergen 1300 Morris Drive Chesterbrook, PA 19087 Questions or Concerns? www.mygnp.com Relabeled By; Proficient Rx LP Thousand Oaks CA 91320 Made in Korea
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients benzalkonium chloride, boric acid, calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, sodium hydroxide
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Directions • Instill 1 or 2 drops in the affected eye(s) as needed.
Purpose
Information about the drug product’s indications for use.Uses • For the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sun. • May be used as a protectant against further irritation.
Spl product data elements
Usually a list of ingredients in a drug product.GNP Lubricating Relief Carboxymethylcellulose Sodium CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM CARBOXYMETHYLCELLULOSE BENZALKONIUM CHLORIDE BORIC ACID CALCIUM CHLORIDE HYDROCHLORIC ACID MAGNESIUM CHLORIDE POTASSIUM CHLORIDE WATER SODIUM BORATE SODIUM CHLORIDE SODIUM HYDROXIDE
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.71205-084-15
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. • If swallowed, get medical help or contact a Poison Control Center right away.
Stop use
Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.Stop use 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.
Storage and handling
Information about safe storage and handling of the drug product.Other information • Use before expiration date marked on container. • Store at 59°-86°F (15°-30°C). • RETAIN THIS CARTON FOR FUTURE REFERENCE.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.Warnings • For external use only. • To avoid contamination, do not touch tip of container to any surface. Replace cap after using. • If solution changes color or becomes cloudy, do not use.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API