NDC 11673-578 Red Eye Relief

Product Information

What is NDC 11673-578?

The NDC code 11673-578 is assigned by the FDA to the product Red Eye Relief which is product labeled by Target Corporation. The product's dosage form is and is administered via form. The product is distributed in a single package with assigned NDC code 11673-578-15 1 bottle, dropper in 1 box / 15 ml in 1 bottle, dropper. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information, RxNorm crosswalk and the complete product label.

NDC Product Code11673-578
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.		Red Eye Relief
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.		Target Corporation
Labeler Code11673
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.		03-04-2015
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.		12-31-2019
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". 		I
NDC Code Structure

What are the uses for Red Eye Relief?


Product Packages

NDC Code 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.

Product Details

Red Eye Relief Active Ingredients UNII Codes

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 indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1235200 - glycerin 0.5 % / naphazoline HCl 0.03 % Ophthalmic Solution
  • RxCUI: 1235200 - glycerin 5 MG/ML / naphazoline hydrochloride 0.3 MG/ML Ophthalmic Solution
  • RxCUI: 1235200 - glycerin 0.5 % / naphazoline hydrochloride 0.03 % Ophthalmic Solution

Red Eye Relief Inactive Ingredients UNII Codes

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.

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Red Eye Relief Product Label

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.

Product Label Table of Contents



Otc - Active Ingredient



Active ingredients                                                Purpose

Glycerin 0.5%................................................... Lubricant

Naphazoline hydrochloride 0.33%........................ Redness Reliever


Otc - Purpose



Uses

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

Warnings



Warnings

For external use only


Otc - Do Not Use



Do not use

  • if solution changes color or becomes cloudy

Otc - Ask Doctor



Ask a doctor before use

  • if you have narrow angle glaucoma

Otc - When Using



When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • replace cap after using
  • overuse may product icreased redness of the eye
  • pupils may become enlarged temporarily

Otc - Stop Use



Stop use and ask a doctor if

  • you experience eye pain
  • you experience changes in vision
  • you experience continued redness of the eye
  • pupils may become enlarged temporarily

Otc - Keep Out Of Reach Of Children



Stop use and ask a doctor if

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



Directions

  • To 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 CORPORATION

MINNEAPOLIS, MN 55403

MADE IN KOREA


Package Label.Principal Display Panel



image description - 578

image description - 578


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