Eyesaline Concentrate

Manufacturer
Protective Industrial Products, Inc.
Effective date
2026-07-02
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
weekly-update
Hydrated at
2026-07-17 21:43:47

Label at a glance#

ProductEyesaline Eyewash Concentrate
Active ingredientWATER
Label structure9 sections

Indications and uses

For flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Dosage and administration

Concentrate must be diluted (1) part concentrate to (10) parts potable water before use • Prepare sufficient quantity of constituted eyewash solution in advance of an emergency. • Mix concentrate with potable water to prepare eyewash solution as follows: • Determine quantity of eyewash solution required • Follow sanitary procedures • Wear protective eyewear and gloves • Pour 1/3 of required amount of potable water...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 92.14%

Purpose

OTC - PURPOSE SECTION

Eyewash

Uses

INDICATIONS & USAGE SECTION

For flushing the eye to remove loose foreign material, air pollutants or chlorinated water

Warnings

WARNINGS SECTION

For external use only- Obtain immediate medical treatment for all open wounds in or near eyes. To avoid contamination, do not touch tip of container to any surface. Replace cap after use.

Do not use

OTC - DO NOT USE SECTION

  • In concentrated form
  • While wearing contact lenses
  • For injection
  • In intraocular sugery
  • Internally
  • if eye is lacerated or object is imbeded
  • if seal is broken

Stop use and consult a doctor if you have

OTC - STOP USE SECTION

  • changes in vision
  • continued redness, irritation or pain, or if the condition worsens or persist

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

  • Concentrate must be diluted (1) part concentrate to (10) parts potable water before use

• Prepare sufficient quantity of constituted eyewash solution in advance of an emergency.
• Mix concentrate with potable water to prepare eyewash solution as follows:
• Determine quantity of eyewash solution required
• Follow sanitary procedures
• Wear protective eyewear and gloves
• Pour 1/3 of required amount of potable water into mixing container or eyewash unit
• Add 1/3 of required amount of concentrate to water
• Agitate or mix thoroughly
• Repeat until required amount of solution is prepared
• Properly dispose of empty bottle after use.
• Do not reuse • Keep bottle upright
• Replace solution no longer than (6) months after mixing

Other Information

OTHER SAFETY INFORMATION

Do not freeze

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Benzalkonium chloride, edetate disodium, sodium chloride, sodium phosphate dibasic, sodium phosphate monobasic

Questions?

OTC - QUESTIONS SECTION

USA: 800-430-5490

Canada: 888-212-7233

Protective Industrial Products, Inc.

25 British American Blvd. Latham, NY 12110

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

70oz Concentrate Artwork70oz Concentrate Artwork170oz Concentrate Artwork170oz Concentrate Artwork

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80716-30080716-300-01, 80716-300-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
Eyesaline Eyewash ConcentratePURIFIED WATERProtective Industrial Products, Inc.558e5926-9027-d3f6-e063-6294a90ab1212026-07-02WarningsExact identifier
ndc (package): 80716-300-01
ndc (package): 80716-300-02
ndc (product): 80716-300
ndc11 (package): 80716030001
ndc11 (package): 80716030002
spl id: 55a3a894-b069-00f5-e063-6294a90af49a
spl set id: 558e5926-9027-d3f6-e063-6294a90ab121

Reported adverse events (FAERS/openFDA)#

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