NDC 0023-6634 Refresh Relieva Preservative Free

Carboxymethylcellulose Sodium And Glycerin

  1. Labeler Index
  2. Allergan, Inc.
  3. NDC: 0023-6634 Refresh Relieva Preservative Free

NDC Product Code 0023-6634

NDC CODE: 0023-6634

Proprietary Name: Refresh Relieva 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 And Glycerin 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

NDC 0023-6634-01

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

NDC 0023-6634-10

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

NDC Product Information

Refresh Relieva Preservative Free with NDC 0023-6634 is a a human over the counter drug product labeled by Allergan, Inc.. The generic name of Refresh Relieva Preservative Free is carboxymethylcellulose sodium and glycerin. The product's dosage form is solution/ drops and is administered via ophthalmic form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1100650.

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 Relieva 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.
  • BORIC ACID (UNII: R57ZHV85D4)
  • CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
  • ERYTHRITOL (UNII: RA96B954X6)
  • LEVOCARNITINE (UNII: 0G389FZZ9M)
  • MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
  • POTASSIUM CHLORIDE (UNII: 660YQ98I10)
  • WATER (UNII: 059QF0KO0R)
  • SODIUM BORATE (UNII: 91MBZ8H3QO)
  • TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
  • HYALURONATE SODIUM (UNII: YSE9PPT4TH)
  • HYDROCHLORIC ACID (UNII: QTT17582CB)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)

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: 07-26-2019 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: 12-31-2022 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 Relieva Preservative Free Product Label Images

Refresh Relieva 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%Glycerin 0.9%

Purpose

Eye lubricantEye lubricant

Uses

  • For the temporary relief of burning and irritation due to the dryness of the eye.For the temporary relief of discomfort due to minor irritations of the eye or exposure to the wind or sun.For use as a protectant against further irritation or to relieve the 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. Prior to first use, bottle must be primed. Please read the “Instructions for Use” on the insert inside of this carton. *If used for dryness and discomfort associated with LASIK, follow your eye doctor’s instructions.

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 AND THE INSERT FOR FUTURE REFERENCE.

Inactive Ingredients

Boric acid; calcium chloride dihydrate; erythritol; levocarnitine; magnesium chloride hexahydrate; potassium chloride; purified water; sodium borate decahydrate; sodium citrate dihydrate; and sodium hyaluronate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

* Please review the disclaimer below.