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OTC products · Product label record

Sodium Chloride drug information

SODIUM CHLORIDE
YYBA CORP · OPHTHALMIC

Product NDC: 73581-707

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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 nameSODIUM CHLORIDE
Labeler / manufacturerYYBA CORP
RouteOPHTHALMIC
Drug classDrug class not supplied in source label
Product NDC73581-707
Label effective date2026-08-20

Official product label reference

Sodium Chloride — YYBA CORP

This page contains 11 source sections for SODIUM CHLORIDE, ophthalmic route. Label set 597f3347-647c-3545-e063-6294a90abab2, version 1.

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

Directions pull down the lower lid of the affected eye

Purpose

Purpose Hypertoncity agent Uses: temporary relief of corneal edema
Dosage and administration — label text
apply a small amount (1/4 inch) of ointment to the inside of the eyelid apply every 3 or 4 hours or as directed by a doctor
Warnings
Warnings For external use only.
Active ingredient
Active ingredient Sodium chloride 5%
Do not use
Do not use except under the advice and supervision of a doctor
While using this medicine
When using this product it may cause temporary burning and irritation replace cap after use to avoid contamination, do not touch tip of container to any surface
When to stop use and seek help
Stop use and ask a doctor if condition worsens or persists for more than 72 hours you experience eye pain, changes in vision, continued redness or irritation of the eye
Child safety
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.
Unclassified section
Other information Store at 15-25 celsius (59-77 farenheit) Keep tightly closed DO NOT FREEZE do not use if difficult to dispense or visible particles are seen in the product serious side effects associated with use of the product may be reported to the phone number provided below Lot No. & Exp. Date: See box or crimp of tube
Inactive ingredient
Inactive ingredients Lanolin, Mineral Oil, Purified Water, White Petrolatum.

Official sources and product identifiers

Substances listed: SODIUM CHLORIDE

RxNorm identifiers: 1298435

Package NDC codes

73581-707-01, 73581-707-03

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.