SODIUM CHLORIDE HYPERTONICITY

Manufacturer
YYBA CORP | Bausch & Lomb Incorporated
Effective date
2026-03-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:51:00

Label at a glance#

ProductSODIUM CHLORIDE HYPERTONICITY
Active ingredientSODIUM CHLORIDE
Label structure10 sections

Indications and uses

temporary relief of corneal edema

Dosage and administration

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 directed by a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium chloride 5%

Purpose

OTC - PURPOSE SECTION

Hypertonicity agent

Uses

INDICATIONS & USAGE SECTION

temporary relief of corneal edema

Warnings

WARNINGS SECTION

For external use only

Do not use
except under the advice and supervision of a doctor.

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

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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 directed by a doctor

Other information

SPL UNCLASSIFIED SECTION

  • store at 15-25 °C (59-77 °F)
  • keep tightly closed
  • DO NOT FREEZE
  • see crimp of tube or carton for Lot Number and Expiration Date
  • 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 

Inactive ingredients

INACTIVE INGREDIENT SECTION

lanolin, mineral oil, purified water, white petrolatum

Questions or comments?

OTC - QUESTIONS SECTION

[phone icon] Call 1-866-933-6337

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

Welmate ®

100%

SATISFACTION

GUARANTEED

NDC 73581-708-35

EYE

OINTMENT

SODIUM CHLORIDE

HYPERTONICITY OPHTHALMIC

OINTMENT, 5%

TEMPORARY RELIEF OF

CORNEAL EDEMA

5%

STERILE

NET WT. 1/8 OZ. (3.5 g)

9805701

WM15842

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1298435sodium chloride 5 % Ophthalmic OintmentPSN5
1298435sodium chloride 0.000855 MEQ/MG Ophthalmic OintmentSCD5
1298435NaCl 0.000855 MEQ/MG Ophthalmic OintmentSY5
1298435NaCl 5 % Ophthalmic OintmentSY5
1298435sodium chloride 50 MG (5 % ) Ophthalmic OintmentSY5

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
SODIUM CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
a21a21e5-f36d-4c1f-8918-def921b8f7e3Product name320250124
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
f1e0dc7e-7d61-4625-b6d9-4894927679d7Product name220211025
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
e4870509-7e28-6f92-f0be-dd3dd889a9cfProduct name520200810
6e9d4a47-c464-b93e-aebc-ad7bffc9c4cdProduct name220190619
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508
5668b646-cd56-c3c7-bdea-3f6b1a8840dbProduct name120140508
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
684ea482-2e8b-14af-5664-b98f1e402036Product name120140508
810ab97e-f109-f41c-7c83-6a652a9cbf43Product name120140508
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
8dbefedf-0a0d-a224-5a3c-66dc9e11c2ddProduct name120140508
b060cc1a-fe47-856b-0b77-4448b5963de8Product name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508
ed912195-5da0-0f2f-6f4b-3ef17710cbe3Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73581-708-35SODIUM CHLORIDE HYPERTONICITY3.5 mL in 1 TUBEOINTMENT3.55
73581-708-35SODIUM CHLORIDE HYPERTONICITY1 in 1 CARTONOINTMENT15

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73581-70873581-708-35

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
SODIUM CHLORIDE HYPERTONICITYSODIUM CHLORIDEYYBA CORP439653b9-99b8-4799-8d67-4a2ada9c67832026-03-20WarningsExact identifier
ndc (package): 73581-708-35
ndc (product): 73581-708
ndc11 (package): 73581070835
spl id: 4d79a117-dffc-b6b4-e063-6294a90a2291
spl set id: 439653b9-99b8-4799-8d67-4a2ada9c6783

Reported adverse events (FAERS/openFDA)#

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