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Carboxymethylcellulose sodium 1% - Medication Information

Product NDC Code 0536-1398
Drug Name

Carboxymethylcellulose sodium 1%

Type Brand
Active Ingredients
Carboxymethylcellulose sodium 10 mg/ml
Route OPHTHALMIC
Dosage Form LIQUID
RxCUI drug identifier 1718952
Application Number M018
Labeler Name RUGBY LABORATORIES
Packages
Package NDC Code Description
0536-1398-81 30 vial, single-use in 1 carton (0536-1398-81) / .4 ml in 1 vial, single-use
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Carboxymethylcellulose sodium 1%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions To open, TWIST AND PULL TAB TO REMOVE . Instill 1 or 2 drops in the affected eye(s) as needed and discard container.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Calcium chloride, Hydrochloric acid, Magnesium chloride, Potassium chloride, Purified water, Sodium chloride, Sodium hydroxide, Sodium lactate.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
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.

Purpose

Information about the drug product’s indications for use.
Purpose Eye lubricant

Spl product data elements

Usually a list of ingredients in a drug product.
Carboxymethylcellulose Sodium 1% carboxymethylcellulose sodium HYDROCHLORIC ACID MAGNESIUM CHLORIDE ANHYDROUS CALCIUM CHLORIDE POTASSIUM CHLORIDE WATER SODIUM CHLORIDE SODIUM LACTATE CARBOXYMETHYLCELLULOSE SODIUM CARBOXYMETHYLCELLULOSE SODIUM HYDROXIDE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PRINCIPAL DISPLAY PANEL Carton

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use Do not use: • If solution changes color or becomes cloudy.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. Keep this and all drugs out of the reach of children . If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Other information • Store at 59°-86° F (15°-30°C) • Use only if single-use container is intact. Questions or comments? Call (888) 969-6855

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if • You experience eye pain, changes in vision, continued redness, or irritation of the eye. • The condition worsens or persists for more than 72 hours.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings • For use in eyes only. • Using this product, to avoid contamination, do not touch tip of container to any surface. • Do not reuse. Once opened, discard after use. • Do not touch single-use container tip to the eye. Stop use and ask a doctor if • You experience eye pain, changes in vision, continued redness, or irritation of the eye. • The condition worsens or persists for more than 72 hours. Keep out of reach of children. Keep this and all drugs out of the reach of children . If swallowed, get medical help or contact a Poison Control Center immediately (1-800-222-1222).

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API