NDC 49668-001 Carboxymethylcellulose Sodium

  1. Labeler Index
  2. Promed Exports Private Limited
  3. NDC: 49668-001 Carboxymethylcellulose Sodium

NDC Product Code 49668-001

NDC CODE: 49668-001

Proprietary Name: Carboxymethylcellulose Sodium 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: 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

  • 49668 - Promed Exports Private Limited

NDC 49668-001-01

Package Description: 30 VIAL, SINGLE-DOSE in 1 CONTAINER > .4 mL in 1 VIAL, SINGLE-DOSE

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

NDC Product Information

Carboxymethylcellulose Sodium with NDC 49668-001 is a product labeled by Promed Exports Private Limited. The generic name of Carboxymethylcellulose Sodium is . The product's dosage form is and is administered via form.

Labeler Name: Promed Exports Private Limited

Dosage Form: -

Product Type: 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.

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

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Promed Exports Private Limited
Labeler Code: 49668
Start Marketing Date: 10-01-2009 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: 12-31-2017 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 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.

Carboxymethylcellulose Sodium Product Label Images

Carboxymethylcellulose Sodium 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 Ingredient

Carboxymethylcellulose sodium (CMC) 0.5% ............... Eye lubricant

Uses

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

Warnings

  • For external use only.To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.Do not touch unit-dose tip to eye.Do not use if solution changes color or becomes cloudy.

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

To open, TWIST AND PULL TAB TO REMOVE. Instill 1 or 2 drops in the affected eye(s) as needed and discard container.If used for post-operative (e.g. LASIK) dryness and discomfort, follow your eye doctor’s instructions.

Other Information

  • Use only if single-use container is intact. RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive Ingredients

Calcium chloride; magnesium chloride; potassium chloride; purified water; sodium chloride; and sodium lactate. May also contain hydrochloric acid and/or sodium hydroxide to adjust pH.

* Please review the disclaimer below.