Redicare Emergency First Aid Eyewash

Manufacturer
Redicare LLC
Effective date
2017-11-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:10:14

Label at a glance#

ProductRedicare Emergency First Aid Eyewash
Active ingredientWATER
Label structure8 sections

Indications and uses

■ for flushing the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination.

Dosage and administration

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

Storage and handling

Store at room temperature 5˚C to 35˚C (41F˚ to 95˚F).

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Purified Water 98.3%

Purpose

OTC - PURPOSE SECTION

Emergency First Aid Eyewash

Uses

INDICATIONS & USAGE SECTION

■ for flushing the eye to reduce chances of severe injury caused by acid, alkali, or particulate contamination.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

■ for injection ■ in intraocular surgery internally ■ internally ■ if solution changes color or becomes cloudy

Ask a doctor if you have

OTC - ASK DOCTOR SECTION

■ eye pain ■ changes in vision ■ redness or irritation of the eye after use ■ an injury caused by an alkali

OTHER SAFETY INFORMATION

To avoid contamination, do not touch tip of container to any surface. Do not reuse. Once opened, discard.

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

STORAGE AND HANDLING SECTION

Store at room temperature 5˚C to 35˚C (41F˚ to 95˚F).

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Sodium chloride, sodium borate, boric acid, sorbic Acid.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

eye washeye wash

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
71105-00071105-000-01, 71105-000-02

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
5df33082-7ef2-825c-e053-2a91aa0adf575da0e918-9a67-4091-e053-2a91aa0abd242017-11-14WarningsExact identifier
spl id: 5df33082-7ef2-825c-e053-2a91aa0adf57
spl set id: 5da0e918-9a67-4091-e053-2a91aa0abd24

Reported adverse events (FAERS/openFDA)#

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