NDC 0023-6952 Refresh Digital

Carboxymethylcellulose Sodium, Glycerin, Polysorbate 80

NDC Product Code 0023-6952

NDC 0023-6952-10

Package Description: 1 BOTTLE, DROPPER in 1 CARTON > 10 mL in 1 BOTTLE, DROPPER

NDC Product Information

Refresh Digital with NDC 0023-6952 is a a human over the counter drug product labeled by Allergan, Inc.. The generic name of Refresh Digital is carboxymethylcellulose sodium, glycerin, polysorbate 80. The product's dosage form is solution/ drops and is administered via ophthalmic form.

Labeler Name: Allergan, Inc.

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.

Refresh Digital 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 mg/mL
  • GLYCERIN 10 mg/mL
  • POLYSORBATE 80 5 mg/mL

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.

  • BORIC ACID (UNII: R57ZHV85D4)
  • CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
  • CASTOR OIL (UNII: D5340Y2I9G)
  • ERYTHRITOL (UNII: RA96B954X6)
  • LEVOCARNITINE (UNII: 0G389FZZ9M)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SODIUM CHLORITE (UNII: G538EBV4VF)

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: Allergan, Inc.
Labeler Code: 0023
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: 08-01-2020 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: 12-31-2021 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 - NO 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.

Refresh Digital 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

Purpose

Carboxymethylcellulose sodium 0.5%............................................................Eye lubricantGlycerin 1%.....................................................................................................Eye lubricantPolysorbate 80 0.5% ..................................................................................... Eye lubricant

Uses

  • For the temporary relief of burning and irritation due to dryness of the eye.For the temporary relief of discomfort due to minor irritations of the eye or exposure to wind or sun.For use as a protectant against further irritation or to relieve dryness of the eye.For use as a lubricant to prevent further irritation or to relieve dryness of the eye.

Warnings

  • For external use only.To avoid contamination, do not touch tip of container to any surface. Replace cap after using.If solution changes color, do not use.

Stop Use And Ask A Doctor

If you experience eye pain, changes in vision, continued redness or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Instill 1 or 2 drops in the affected eye(s) as needed.

Other Information

  • Use only if tape seals on top and bottom flaps are intact. Use before expiration date marked on container. Discard 90 days after opening.Store at 59°-86°F (15°-30°C).RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive Ingredients

Boric acid; carbomer copolymer type A; castor oil; erythritol; levocarnitine; purified water;PURITE® (stabilized oxychloro complex); and sodium hydroxide.

* Please review the disclaimer below.