NDC 59779-337 Eye Wash


NDC Product Code 59779-337

NDC 59779-337-09

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 118 mL in 1 BOTTLE, PLASTIC

NDC Product Information

Eye Wash with NDC 59779-337 is a a human over the counter drug product labeled by Cvs Pharmacy. The generic name of Eye Wash is water. The product's dosage form is solution and is administered via ophthalmic form.

Labeler Name: Cvs Pharmacy

Dosage Form: Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Eye Wash Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • WATER 99.05 mL/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.


Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Ophthalmic - Administration to the external eye.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Cvs Pharmacy
Labeler Code: 59779
FDA Application Number: part349 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 08-31-2010 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2021 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N - NO What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Eye Wash Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Purified water (99.05%)




  • Washes the eye to help relieve •irritation •stinging •discomfort •itching •burningby removing •loose foreign material •air pollutants (smog or pollen) •chlorinated water


For external use only

Do Not Use

  • •if you have open wounds in or near the eyes, and get medical help right away •if solution changes color or becomes cloudy

When Using This Product

  • •remove contact lenses before using •do not touch tip of container to any surface to avoid contamination •replace cap after use

Stop Use And Ask A Doctor If

  • •you experience eye pain, changes in vision, continued redness or irritation of the eye •condition worsens or persists

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.


  • For use with a nozzle applicator. •flush the affected eye(s) as needed •control the rate of flow of solution by pressure on the bottle •do not touch dropper tip to eye

When Using An Eye Cup

  • •rinse the cup with Soothing Eye Wash Solutionimmediately before each use •avoid contamination of the rim and insidesurfaces of the cup •fill the cup half full with Soothing Eye WashSolution and apply the cup to the affected eye(s),pressing tightly to prevent spillage

Other Information

  • •store at 15°-25°C (59°-77°F) •keep tightly closed •does not contain thimerosal •enclosed eyecup is sterile if packaging is intact •use before expiration date marked on thecarton or bottle

Inactive Ingredients

Boric acid, sodium borate and sodium chloride. PRESERVATIVE ADDED: benzalkonium chloride(0.01%)

* Please review the disclaimer below.