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Sunmark lubricating tears - Medication Information

Product NDC Code 49348-149
Drug Name

Sunmark lubricating tears

Type Brand
Active Ingredients
Polyethylene glycol 400 .4 g/100ml
Propylene glycol .3 g/100ml
Route OPHTHALMIC
Dosage Form SOLUTION/ DROPS
RxCUI drug identifier 477589
Application Number M018
Labeler Name Strategic Sourcing Services LLC
Packages
Package NDC Code Description
49348-149-29 1 bottle, plastic in 1 carton (49348-149-29) / 15 ml in 1 bottle, plastic
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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 children under 6 years of age: ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Benzalkonium chloride as preservative, boric acid, calcium chloride, hypromellose, magnesium chloride, potassium chloride, purified water, sodium borate, sodium chloride, zinc chloride

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 and irritation due to dryness of the eye

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Sunmark Lubricating Tears Polyethylene glycol 400, Propylene glycol BENZALKONIUM CHLORIDE BORIC ACID CALCIUM CHLORIDE HYPROMELLOSES MAGNESIUM CHLORIDE POTASSIUM CHLORIDE WATER SODIUM BORATE SODIUM CHLORIDE ZINC CHLORIDE POLYETHYLENE GLYCOL 400 POLYETHYLENE GLYCOL 400 PROPYLENE GLYCOL PROPYLENE GLYCOL

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.
Carton

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
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

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 product 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 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 RETAIN THIS CARTON FOR FUTURE REFERENCE Store at room temperature

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 the tip of the container to any surface to avoid contamination replace cap after each 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 product changes color or becomes cloudy if you are sensitive to any ingredient in this product When using this product do not touch the tip of the 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 Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center 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