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Walgreens lubricant eye drops - Medication Information

Product NDC Code 0363-2112
Drug Name

Walgreens lubricant eye drops

Type Brand
Active Ingredients
Propylene glycol .06 mg/ml
Route OPHTHALMIC
Dosage Form SOLUTION/ DROPS
Application Number part349
Labeler Name WALGREEN COMPANY
Packages
Package NDC Code Description
0363-2112-15 2 bottle, dropper in 1 carton (0363-2112-15) / 10 ml in 1 bottle, dropper
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Purpose Propylene Glycol 0.6% Lubricant
Active IngredientsPurpose
Propylene Glycol 0.6%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.
Directions • Shake well. • Wash your hands. • Instill 1 or 2 drops in the affected eye(s) as needed.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Highly purified water, Boric acid, Hypromellose, Sodium borate, Sodium chloride, Calcium chloride, Benzalkonium chloride, Potassium chloride, Disodium edetate, Magnesium chloride, HCI 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 relief of dryness of the eye, and protectant against further irritation of the eye. For temporary relief of buming, irritation, and discomfort including exposure to wind or sun.

Spl product data elements

Usually a list of ingredients in a drug product.
Walgreens Lubricant Eye Drops propylene glycol BORIC ACID EDETATE DISODIUM HYPROMELLOSES CALCIUM CHLORIDE WATER HYDROCHLORIC ACID MAGNESIUM CHLORIDE SODIUM BORATE PROPYLENE GLYCOL PROPYLENE GLYCOL BENZALKONIUM CHLORIDE SODIUM CHLORIDE POTASSIUM CHLORIDE

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.
PRINCIPAL DISPLAY PANEL Carton Label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information • Use only if imprinted tape seals on top and bottom flaps are intact and clearly legible. • Use before expiration date marked on container. • Discard 30 days after opening. • Store at 59°-86° F (15°-30°C).

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 (1-800-222-1222) right away.

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? 1-800-925-4733 9 am to 5 pm EST; Monday - Friday.

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 any of the following: • You experience eye pain, changes in vision, continued redness or irritation of the eye. • The condition 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 • Retain outer carton for full product drug facts. • To avoid contamination, do not touch tip of container to any surface. Close cap after using. • If solution changes color or becomes cloudy, do not use.

Pregnancy or breast feeding

Pregnancy or Breast feeding
Pregnancy or Breast Feeding • If pregnant or breast feeding , ask a health professional before use.

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 use in eyes only. ​• For external use only. • Retain outer carton for full product drug facts. • To avoid contamination, do not touch tip of container to any surface. Close cap after using. • If solution changes color or becomes cloudy, do not use. When using this product • Retain outer carton for full product drug facts. • To avoid contamination, do not touch tip of container to any surface. Close cap after using. • If solution changes color or becomes cloudy, do not use. Stop use and ask a doctor if you experience any of the following: • You experience eye pain, changes in vision, continued redness or irritation of the eye. • The condition 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 (1-800-222-1222) right away. Pregnancy or Breast Feeding • If pregnant or breast feeding , ask a health professional before 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