Walgreens Sodium Chloride Ointment 0.125 oz NBE Muro 128

Manufacturer
Walgreen Company
Effective date
2018-04-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:58:21

Label at a glance#

ProductWalgreens Hypertonicity
Active ingredientSODIUM CHLORIDE
Label structure13 sections

Storage and handling

Other information store between 15-25°C (59-77°F) do not freeze keep tightly closed do not roll, bend, twist or fold tube during use as this may cause the tube to tear or crack

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Sodium chloride 5%...........................................................Eye hypertonicity agent

OTC - PURPOSE SECTION

Use

  • temporary relief of corneal edema

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use

  • except under the advice and supervision of a doctor
  • if difficult to dispense or visible particles are seen in the product

OTC - WHEN USING SECTION

When using this product

  • it may cause temporary burning and irritation when instilled into the eye
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after each use
  • remove contact lense before using

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • you feel eye pain
  • changes in vision occur
  • redness or irritation of the eye lasts
  • condition worsens or lasts more than 72 hours

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

INDICATIONS & USAGE SECTION

Directions

  • pull down the lower lid of the affected eye
  • apply a small amount (1/4 inch) of ointment to the inside of eyelid
  • apply every 3 or 4 hours or as a directed by a doctor

STORAGE AND HANDLING SECTION

Other information

  • store between 15-25°C (59-77°F)
  • do not freeze
  • keep tightly closed
  • do not roll, bend, twist or fold tube during use as this may cause the tube to tear or crack

INACTIVE INGREDIENT SECTION

Inactive ingredients

lanolin, mineral oil, purified water, white petrolatum

DOSAGE & ADMINISTRATION SECTION

Distributed by:

200 Wilmot Rd.

Deerfield, IL 60015

Made in South Korea

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

placeplace

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-15730363-1573-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
cddf7d2c-6e31-7104-e053-2995a90ae7896997ed2a-b23e-25e6-e053-2991aa0a35572021-10-08WarningsExact identifier
spl set id: 6997ed2a-b23e-25e6-e053-2991aa0a3557

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.