NDC 11673-578 Red Eye Relief

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  2. Target Corporation
  3. NDC: 11673-578 Red Eye Relief

NDC Product Code 11673-578

NDC CODE: 11673-578

Proprietary Name: Red Eye Relief 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.

NDC Code Structure

  • 11673 - Target Corporation

NDC 11673-578-15

Package Description: 1 BOTTLE, DROPPER in 1 BOX > 15 mL in 1 BOTTLE, DROPPER

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Red Eye Relief with NDC 11673-578 is a product labeled by Target Corporation. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1235200.

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.
  • BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
  • BORIC ACID (UNII: R57ZHV85D4)
  • SODIUM BORATE (UNII: 91MBZ8H3QO)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Target Corporation
Labeler Code: 11673
Start Marketing Date: 03-04-2015 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: 12-31-2019 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Red Eye Relief Product Label Images

Red Eye Relief 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

Otc - Active Ingredient

Active ingredients                                                PurposeGlycerin 0.5%................................................... LubricantNaphazoline hydrochloride 0.33%........................ Redness Reliever

Otc - Purpose

  • UsesFor the relief of redness of the eye due to minor eye irritationsFor the temporary relief of burning and irritation due to dryness of the eyeFor use as a protectant against futher irritation or to relive dryness of the eye

Warnings

WarningsFor external use only

Otc - Do Not Use

  • Do not useif solution changes color or becomes cloudy

Otc - Ask Doctor

  • Ask a doctor before useif you have narrow angle glaucoma

Otc - When Using

  • When using this productto avoid contamination, do not touch tip of container to any surfacereplace cap after usingoveruse may product icreased redness of the eyepupils may become enlarged temporarily

Otc - Stop Use

  • Stop use and ask a doctor ifyou experience eye painyou experience changes in visionyou experience continued redness of the eyepupils may become enlarged temporarily

Otc - Keep Out Of Reach Of Children

  • Stop use and ask a doctor ifyou experience eye painyou experience changes in visionyou experience continued redness or irritation of the eyethe condition worsenssymptoms persist for more than 72 hours

Indications & Usage

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Storage And Handling

  • DirectionsTo open bottle, push cap down and twist counterclockwise. To close bottle, twist clockwise until it stops turning

Inactive Ingredient

Inactive ingredients:Benzalkonium Choride, Boric Acid, Disodium Edetate Hydrate, Sodium Borate, Sterile Purified Water

Dosage & Administration

DISTRIBUTED BY:TARGET CORPORATIONMINNEAPOLIS, MN 55403MADE IN KOREA

* Please review the disclaimer below.