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Cvs lubricant eye drops ultra - Medication Information

Product NDC Code 69842-752
Drug Name

Cvs lubricant eye drops ultra

Type Brand
Active Ingredients
Polyethylene glycol 400 .4 g/100ml
Propylene glycol .3 g/100ml
Route OPHTHALMIC
Dosage Form SOLUTION
RxCUI drug identifier 477589
Application Number M018
Labeler Name CVS
Packages
Package NDC Code Description
69842-752-01 30 vial, single-use in 1 carton (69842-752-01) / .4 ml in 1 vial, single-use
69842-752-02 60 vial, single-use in 1 carton (69842-752-02) / .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 ingredients Polyethylene glycol 400.........0.4% Propylene glycol ...................0.3%

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 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 boric acid, hydrochloric acid**, hypromellose, potassium chloride, purified water, sodium chloride, sodium hydroxide** ** May contain these ingredients 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.
Use for the temporary relief of burning and irritation of the eye due to dryness of the eye

Purpose

Information about the drug product’s indications for use.
Purposes Polyethylene glycol 400......Lubricant Propylene glycol.................Lubricant

Spl product data elements

Usually a list of ingredients in a drug product.
CVS Lubricant Eye Drops Ultra Polyethylene glycol 400, Propylene glycol POTASSIUM CHLORIDE SODIUM HYDROXIDE PROPYLENE GLYCOL PROPYLENE GLYCOL HYDROCHLORIC ACID HYPROMELLOSE, UNSPECIFIED BORIC ACID SODIUM CHLORIDE POLYETHYLENE GLYCOL 400 POLYETHYLENE GLYCOL 400 WATER

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.
60 ct carton 30 ct carton

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 this solution changes color or becomes cloudy if you are sensitive to any ingredient in this product

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.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information store at 15º-25º C (59º-77º F) use only if single-use container is intact use before expiration date marked on container RETAIN THIS CARTON FOR FUTURE REFERENCE

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 feel eye pain changes in vision occur redness or irritation of the eye(s) gets worse or lasts 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 do not touch tip of container to any surface to avoid contamination replace cap after each use

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 external use only Do not use if this solution changes color or becomes cloudy if you are sensitive to any ingredient in this product When using this product do not touch tip of container to any surface to avoid contamination replace cap after each use Stop use and ask a doctor if you feel eye pain changes in vision occur redness or irritation of the eye(s) gets worse or lasts more than 72 hours If pregnant or breast-feeding, ask a health professional before use Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

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