NDC 11673-150 Lubricant Eye Drops Preservative Free

Carboxymethylcellulose Sodium

NDC Product Code 11673-150

NDC Code: 11673-150

Proprietary Name: Lubricant Eye Drops Preservative Free 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.

Non-Proprietary Name: Carboxymethylcellulose Sodium 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.

NDC Code Structure

  • 11673 - Target Corporation
    • 11673-150 - Lubricant Eye Drops Preservative Free

NDC 11673-150-01

Package Description: 70 VIAL, DISPENSING in 1 BOX > .4 mL in 1 VIAL, DISPENSING

NDC Product Information

Lubricant Eye Drops Preservative Free with NDC 11673-150 is a a human over the counter drug product labeled by Target Corporation. The generic name of Lubricant Eye Drops Preservative Free is carboxymethylcellulose sodium. The product's dosage form is solution/ drops and is administered via ophthalmic form.

Labeler Name: Target Corporation

Dosage Form: Solution/ Drops - A solution which is usually administered in a drop-wise fashion.

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.

Lubricant Eye Drops Preservative Free 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.


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)

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: Target Corporation
Labeler Code: 11673
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: 02-12-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Lubricant Eye Drops Preservative Free Product Label Images

Lubricant Eye Drops Preservative Free 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 ingredientCarboxymethylcellulose sodium 0.5%

Otc - Purpose

PurposeCarboxymethylcellulose sodium.............Lubricant

Indications & Usage

  • Usesfor the temporary relief of burning, irritation, and discomfort due to dryness of the eye or exposure to wind or sunmay be used as a protectant against further irritation


​WarningsFor external use only.

Otc - Do Not Use

​Do not use if solution changes color or becomes cloudy.

Otc - When Using

  • When using the productdo not reuseonce opened, discardto avoid contamination do not touch tip of container to any surfacedo not touch unit-dose tip to eye.

Otc - Stop Use

  • Stop use and ask a doctor ifyou experience eye painchanges in vision occurredness or irritation of the eye continuesredness or irritation of the eye worsens or persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Dosage & Administration

  • DirectionsTo open, twist and pull tab to removeInstill 1 or 2 drops in the affected eye(s) as needed and discard containerIf used for post-operative (e.g., LASIK) dryness and discomfort, follow your eye doctor’s instructions.

Other Safety Information

  • Other informationStore at 15°-25°C (59°-77°F)Use only if single-use container is intactUse before expiration date marked on containerRETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive Ingredient

Inactive ingredientsCalcium chloride, magnesium chloride, potassium chloride, purified water, sodiumchloride, and sodium lactate. May contain sodium hydroxide and/or hydrochloric acidto adjust pH.

* Please review the disclaimer below.

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