NDC 63868-969 Quality Choice Lubricating Eye Drops

NDC Product Code 63868-969

NDC 63868-969-15

Package Description: 1 BOTTLE in 1 CARTON > 15 mL in 1 BOTTLE

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

NDC Product Information

Quality Choice Lubricating Eye Drops with NDC 63868-969 is a product labeled by Chain Drug Marketing Association Inc. The generic name of Quality Choice Lubricating Eye Drops is . The product's dosage form is and is administered via form.

Labeler Name: Chain Drug Marketing Association Inc

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.

  • 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: Chain Drug Marketing Association Inc
Labeler Code: 63868
Start Marketing Date: 09-30-2012 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.

Quality Choice Lubricating Eye Drops Product Label Images

Quality Choice Lubricating Eye Drops 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

ingredients------------------------------------------------PurposeCarboxymethylcellulose Sodium 0.5%-------------------LubricantGlycerin

Otc - Purpose

  • UsesFor the temporary relief of burning, irritation and discomfort due to
  • Dryness of the eye or from irritation from wind or sun.


  • WarningsFor external use only

Otc - When Using

  • When using this productTo avoid contamination, do not touch tip of container to any surface.
  • Replace cap after using.
  • Do not use if solution changes color or gets cloudy.

Otc - Stop Use

Stop use and ask a doctor if You feel eye pain, changes in vision, continued redness, or irritation of the
eye, or if the condition worsens or persists for more than 72

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

DirectionsPut 1 or 2 drops in the affected eye/s as needed.

Storage And Handling

  • Other informationsome users may experience a brief tingling sensationStore at room temperature.

Inactive Ingredient

Inactive ingredients: Boric Acid, Sodium Borate, Levocarnitin, Potassium Chloride, Calcium Chloride Dihydrate, Magnesium Chloride, Erythritol, Sodium Citrate Dihydrate, Potassium Sorbate, Purified Water

Dosage & Administration

Distributed by C.D.M.A., Inc.43157 W. Nine MileNovi, MI 48376-0995www.qualitychoice.comMade in Korea

* Please review the disclaimer below.