NDC 59779-337 Eye Wash
Water Solution Ophthalmic

Product Information

Product Code59779-337
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Eye Wash
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Product Type 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.
Human Otc Drug
Dosage FormSolution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
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.
Cvs Pharmacy
Labeler Code59779
FDA Application Number 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 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.
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date 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 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 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".
NDC Code Structure

Usage Information

Product Packages

NDC 59779-337-09

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

Product Details

Eye Wash is 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.

What are Eye Wash Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

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.


* Please review the disclaimer below.

Eye Wash Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents

Active Ingredient

Purified water (99.05%)




washes the eye to help relieve

  • •irritation
  • •stinging
  • •discomfort
  • •itching
  • •burning
  • by 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 Solution

    immediately before each use

  • •avoid contamination of the rim and inside

    surfaces of the cup

  • •fill the cup half full with Soothing Eye Wash

    Solution 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 the

    carton or bottle

Inactive Ingredients

boric acid, sodium borate and sodium chloride. PRESERVATIVE ADDED: benzalkonium chloride


Questions Or Comments?

Call: 1-866-767-9161

Package/Label Principal Display Panel



Eye Wash



For daily or emergency

eye cleansing

• Cleanses

• Refreshes

• Soothes

• Sterile eye cup


[icon] blue heart with drop inside


4 FL OZ (118 mL)

* Please review the disclaimer below.