Eye Wash

Manufacturer
M-star (Hubei) Health&Care Products Co., Ltd.
Effective date
2024-04-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:12:28

Label at a glance#

ProductEye Wash
Active ingredientWATER
Label structure9 sections

Dosage and administration

Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 99.1%

Purpose

OTC - PURPOSE SECTION

Eyewash

Use

INDICATIONS & USAGE SECTION

  • For cleansing the eye to help relieve irritation or burning by removing loose foreign material 

Warnings

WARNINGS SECTION

For external use only. 

Do not use

OTC - DO NOT USE SECTION

if solution changes color or become cloudy 

when using this products

OTC - WHEN USING SECTION

  • to avoid contamination,do not touch tip of container to any surface do not reuse
  • once opened, discard
  • obtain immediate medical treatment 
  • for all open wounds in or near the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • eye pain
  • changes in vision
  • continued redness 
  • irritation of the eye
  • condition worsens or persists

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

  • Flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Other information

SPL UNCLASSIFIED SECTION

  • not for use as contact lens solution 
  • Use before expiration date marked on the bottle 
  • Store at room temperature,5°C to 35°C 

Inactive ingredients

INACTIVE INGREDIENT SECTION

sodium chloride

To report a serious adverse event.

OTC - QUESTIONS SECTION

contact +1(855)924-2182

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5.jpgLabel5.jpg

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6.jpgLabel6.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1053429water 99.1 % Ophthalmic Irrigation SolutionPSN1
1053429water 991 MG/ML Ophthalmic Irrigation SolutionSCD1
1053429water 99.05 % Ophthalmic Irrigation SolutionSY1
1053429water 99.1 % Ophthalmic Irrigation SolutionSY1
1053429water 99.1 ML per 100 ML Ophthalmic Irrigation SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84219-007-15Eye Wash15 mL in 1 BOTTLELIQUID151
84219-007-30Eye Wash30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84219-007EYE WASH (WATER) LIQUID [M-STAR (HUBEI) HEALTH&CARE PRODUCTS CO., LTD.]1Current NDC, 2 package rows20240515_71706039-e250-4f08-9687-71b2928c4e46.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84219-00784219-007-15, 84219-007-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RACTIB

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
Eye WashWATERM-star (Hubei) Health&Care Products Co., Ltd.71706039-e250-4f08-9687-71b2928c4e462024-04-01WarningsExact identifier
ndc (package): 84219-007-30
ndc (package): 84219-007-15
ndc (product): 84219-007
ndc11 (package): 84219000715
ndc11 (package): 84219000730
spl id: 1507ac3e-81f1-892c-e063-6394a90ac565
spl set id: 71706039-e250-4f08-9687-71b2928c4e46

Reported adverse events (FAERS/openFDA)#

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