NDC 0363-8800 Walgreens Lubricant Eye Drops Preservative Free

Carboxymethylcellulose Sodium

NDC Product Code 0363-8800

NDC CODE: 0363-8800

Proprietary Name: Walgreens 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • This medication is used to relieve dry, irritated eyes. Common causes for dry eyes include wind, sun, heating/air conditioning, computer use/reading, and certain medications. This product may contain 1 or more of the following ingredients: carboxymethylcellulose, dextran, glycerin, hypromellose, polyethylene glycol 400 (PEG 400), polysorbate, polyvinyl alcohol, povidone, or propylene glycol, among others. Eye lubricants keep the eye moist, help to protect the eye from injury and infection, and decrease symptoms of dry eyes such as burning, itching, and feeling as if something is in the eye.

NDC Code Structure

NDC 0363-8800-01

Package Description: 30 VIAL, SINGLE-USE in 1 BOX > .4 mL in 1 VIAL, SINGLE-USE

NDC 0363-8800-02

Package Description: 70 VIAL, SINGLE-USE in 1 BOX > .4 mL in 1 VIAL, SINGLE-USE

NDC Product Information

Walgreens Lubricant Eye Drops Preservative Free with NDC 0363-8800 is a a human over the counter drug product labeled by Walgreen Company. The generic name of Walgreens Lubricant Eye Drops Preservative Free is carboxymethylcellulose sodium. The product's dosage form is liquid and is administered via ophthalmic form.

Labeler Name: Walgreen Company

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Walgreens 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.

  • CARBOXYMETHYLCELLULOSE SODIUM .5 g/100mL

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.

  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
  • HYDROCHLORIC ACID (UNII: QTT17582CB)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)

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.
  • 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: Walgreen Company
Labeler Code: 0363
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: 12-01-2019 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.

Walgreens 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

Active Ingredients

​Carboxymethylcellulose sodium 0.5%

Purpose

Lubricant

Uses

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

Warnings

For external use only

Do Not Use This Product If

  • Solution changes color or becomes cloudy

When Using This Product

  • Do not reuseonce opened, discardto avoid contamination, do not touch tip of container to any surfacedo not touch unit-dose tip to eye

Stop Use And Ask A Doctor If

  • You 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

Keep Out Of The Reach Of Children.

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

Directions

  • To 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 Information

  • Store at 15°-25ºC (59°-77°F)use only if single-use container is intactuse before expiration date marked on containerRETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive Ingredients

Calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate, **May contain these ingredients to adjust pH.

* Please review the disclaimer below.