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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Allergan, Inc. for the product Refresh Liquigel (NDC 0023-9205). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding other, active ingredient, purpose, uses, warnings, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Carboxymethylcellulose sodium 1%
Eye lubricant
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.
Instill 1 or 2 drops in the affected eye(s) as needed.
Boric acid; calcium chloride; magnesium chloride; potassium chloride; purified water; PURITE® (stabilized oxychloro complex); sodium borate; and sodium chloride.
1.800.433.8871
refreshbrand.com
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
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