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Lubricant eye plus - Medication Information

Product NDC Code 11822-0323
Drug Name

Lubricant eye plus

Type Brand
Active Ingredients
Carboxymethylcellulose sodium, unspecified form .5 g/100ml
Route OPHTHALMIC
Dosage Form SOLUTION/ DROPS
RxCUI drug identifier 1188426
Application Number M018
Labeler Name Rite Aid Corporation
Packages
Package NDC Code Description
11822-0323-1 6 pouch in 1 carton (11822-0323-1) / 5 vial, single-use in 1 pouch / .4 ml in 1 vial, single-use
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each single-use container) Carboxymethylcellulose sodium 0.5%

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.
Directions • to open, twist and pull tab to remove • instill 1 or 2 drops in the affected eye(s) as needed and discard container

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients calcium chloride dihydrate, magnesium chloride hexahydrate, potassium chloride, sodium chloride, sodium lactate solution, water for injection. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

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.
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

Purpose

Information about the drug product’s indications for use.
Purpose Eye lubricant

Spl product data elements

Usually a list of ingredients in a drug product.
Lubricant Eye Plus carboxymethylcellulose sodium CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM CARBOXYMETHYLCELLULOSE CALCIUM CHLORIDE MAGNESIUM CHLORIDE POTASSIUM CHLORIDE SODIUM CHLORIDE SODIUM LACTATE WATER SODIUM HYDROXIDE HYDROCHLORIC ACID

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.
Package/Label Principal Display Panel FREE FROM | PRESERVATIVE FREE Compare to the active ingredient of Refresh Plus ® Lubricant Eye Drops MOISTURIZING RELIEF ACTUAL SIZE LUBRICANT EYE DROPS PLUS CARBOXYMETHYLCELLULOSE SODIUM 0.5% Instantly moisturizes & relieves dry, irritated eyes For sensitive eyes 30 SINGLE-USE CONTAINERS 0.01 FL OZ (0.4 mL) each Sterile 323-83-lubricant-eyedrops-plus

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use if solution changes color or becomes cloudy

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 (1-800-222-1222).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? 1-800-719-9260

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 occur • redness or irritation of the eye continues • redness or irritation of the eye worsens or persists for more than 72 hours

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product to avoid contamination • do not touch tip of container to any surface • do not reuse • once opened, discard • do not touch unit-dose tip to eye

Storage and handling

Information about safe storage and handling of the drug product.
Other information • store at 20-25°C (68-77°F) • 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 Do not use if solution changes color or becomes cloudy When using this product to avoid contamination • do not touch tip of container to any surface • do not reuse • once opened, discard • do not touch unit-dose tip to eye Stop use and ask a doctor if • you experience eye pain • changes in vision occur • redness or irritation of the eye continues • redness or irritation of the eye worsens or persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away (1-800-222-1222).

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