Active Ingredient
Sodium Chloride 5%
The following Structured Product Label (SPL) was submitted to the FDA by Cvs Pharmacy for the product Sodium Chloride (NDC 59779-303). 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 active ingredient, purpose, use, warnings, stop use and ask a doctor if, keep out of the reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Sodium Chloride 5%
Hypertonicity agent
For temporary relief of corneal edema.
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.
If swallowed, get medical help or contact a Poison Control Center right away.
Apply small amount (one-fourth inch) to the inside of affected eye(s) every 3 to 4 hours, or as directed by a doctor.
Mineral Oil, Modified Lanolin, Purified Water and White Petrolatum.
Principal Display Panel Text for Container Label:
CVS Health™ Logo NDC 59779-303-01
Sodium Chloride USP, 5%
HYPERTONICITY OPHTHALMIC OINTMENT
NET WT 0.125 OZ (3.5 g) STERILE
Principal Display Panel Text for Carton Label:
CVS Health™ Logo Compare to the active
ingredient in Muro® 128*
Sodium Chloride, NDC 59779-303-01
USP, 5%
HYPERTONICITY OPHTHALMIC OINTMENT
Temporary relief of corneal edema
NET WT 0.125 OZ (3.5 g) STERILE
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