Start a conversation
Home/Communities/Refresh Liquigel
Re

OTC products · Product label record

Refresh Liquigel drug information

CARBOXYMETHYLCELLULOSE SODIUM
Allergan, Inc. · OPHTHALMIC

Product NDC: 0023-9205

Join the community
CommunityExperiencesReviewsDrug database
Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameCARBOXYMETHYLCELLULOSE SODIUM
Labeler / manufacturerAllergan, Inc.
RouteOPHTHALMIC
Drug classDrug class not supplied in source label
Product NDC0023-9205
Label effective date2026-08-28

Official product label reference

Refresh Liquigel — Allergan, Inc.

This page contains 10 source sections for CARBOXYMETHYLCELLULOSE SODIUM, ophthalmic route. Label set 4b8b2f6a-4b89-446c-9e5b-9b83c453a01d, version 9.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

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

Purpose Eye lubricant
Dosage and administration — label text
Directions Instill 1 or 2 drops in the affected eye(s) as needed.
Warnings
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.
Active ingredient
Active ingredient Carboxymethylcellulose sodium 1%
When to stop use and seek help
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.
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Other safety information
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.
Inactive ingredient
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).
Questions
Questions or comments? 1.800. 6 78 . 1605 refresh eyedrops .com v2.0DFL9205 Telephone

Official sources and product identifiers

Substances listed: CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED

RxNorm identifiers: 579907

Package NDC codes

0023-9205-03, 0023-9205-15, 0023-9205-02

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.