FDA.reportPublic FDA data

EYE WASH

Manufacturer
Guangdong Comfort Medical Products Co., Ltd.
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 20:48:50

Label at a glance#

ProductEYE WASH
Active ingredientWATER
Label structure11 sections

Storage and handling

Store in cool dry place Keep out of direct sunlight Keep out of reach of children

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Purified water (99.1%)..................................... Eyewash

OTC - PURPOSE SECTION

Eye wash

INSTRUCTIONS FOR USE SECTION

  • To pour - hold bottle securely, twist off top to remove
  • Control rate of flow by pressure on the bottle
  • Flush the affected eye(s) as needed
  • Do not touch bottle tip to eye
  • If necessary, continue flushing with emergency eyewash or shower.

WARNINGS SECTION

Do not use if pack is damaged

Do not use resterilize and reuse

DOSAGE & ADMINISTRATION SECTION

Topical irrigation solution

0.9% w/v Sodium Chloride

INDICATIONS & USAGE SECTION

For topical irrigation of eyes, burns and wounds

INACTIVE INGREDIENT SECTION

0.9% w/v Sodium Chloride

OTHER SAFETY INFORMATION

Caution:

Discard any unused solution

Single use only

STORAGE AND HANDLING SECTION

Store in cool dry place

Keep out of direct sunlight

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC# 71584-0107-1

EYE WASH

Topical irrigation solution 0.9% w/v Sodium Chloride

For topical irrigation of eyes, burns and wounds

CAUTION:

DISCARD ANY UNUSED SOLUTION

SINGLE USE ONLY

DO NOT USE IF PACK IS DAMAGED

DO NOT RESTERILIZE AND REUSE

NOT FOR INJECTION

FOR EXTERNAL USE ONLY

STORE IN COOL DRY PLACE

KEEP OUT OF DIRECT SUNLIGHT

KEEP OUT OF REACH OF CHILDREN

20 ml

Made in China

MANUFACTURED FOR:

Total Resources Intenational, Walnut CA 91789. USA

eyewash-1eyewash-1

eyewash-3eyewash-30107-2 label0107-2 label

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
71584-010771584-0107-1, 71584-0107-2, 71584-0107-3

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 CHLORITEG538EBV4VFIACT
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
2edd9c14-b1e5-b606-e063-6394a90a7841548d9fb4-bd57-74c1-e054-00144ff8d46c2025-02-24WarningsExact identifier
spl set id: 548d9fb4-bd57-74c1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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