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Refresh liquigel - Medication Information

Product NDC Code 0023-9205
Drug Name

Refresh liquigel

Type Brand
Active Ingredients
Carboxymethylcellulose sodium 10 mg/ml
Route OPHTHALMIC
Dosage Form GEL
RxCUI drug identifier 579907
Application Number part349
Labeler Name Allergan, Inc.
Packages
Package NDC Code Description
0023-9205-15 1 bottle, dropper in 1 carton (0023-9205-15) / 15 ml in 1 bottle, dropper
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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 Instill 1 or 2 drops in the affected eye(s) as needed.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Boric acid; calcium chloride dihydrate; magnesium chloride hexahydrate; potassium chloride; purified water; PURITE ® (stabilized oxychloro complex); sodium borate decahydrate; and sodium chloride. May contain hydrochloric acid or sodium hydroxide (to adjust pH).

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.
REFRESH LIQUIGEL Carboxymethylcellulose sodium Carboxymethylcellulose sodium Carboxymethylcellulose Boric acid calcium chloride magnesium chloride potassium chloride water sodium borate sodium chloride sodium chlorite HYDROCHLORIC ACID 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 NDC 0023-9205-15 Refresh Liquigel ® Lubricant Eye Gel SOOTHING GEL Long-lasting relief for dry eyes in a soothing gel formula 0.5 fl oz (15 mL) Sterile NDC 0023-9205-15 Refresh Liquigel® Lubricant Eye Gel SOOTHING GEL Long-lasting relief for dry eyes in a soothing gel formula 0.5 fl oz (15 mL) Sterile

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

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
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°-77°F (15°-25°C). RETAIN THIS CARTON FOR FUTURE REFERENCE. Questions or comments? 1.800. 687 . 1605 refreshbrand.com v1.0DFL9205 Telephone

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

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