FDA.reportPublic FDA data

Physicians Care Eyewash

Manufacturer
Acme United Corporation
Effective date
2025-09-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:01

Label at a glance#

ProductPhysicians Care Eyewash
Active ingredientWATER
Label structure11 sections

Dosage and administration

remove tamper evident seal and cap_ 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 98.3%

Purpose

OTC - PURPOSE SECTION

Eyewash

Warnings

WARNINGS SECTION

For external use only

Do not use

  • if you experience any open wounds in or near the eyes and obtain immediate medical treatment
  • if solution changes color or becomes cloudy

When using this product

  • to avoid contamination, do not touch tip of container to any surface
  • do not reuse
  • once opened, discard

Use

INDICATIONS & USAGE SECTION

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

Stop use and ask a doctor if you have any of the following

OTC - ASK DOCTOR SECTION

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

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

  • remove tamper evident seal and cap_
  • flush the affected eye as needed, controlling the rate of flow of solution by pressure on the bottle

Other information

INFORMATION FOR PATIENTS SECTION

  • lot number is printed on the bottle
  • store at 20° to 25° C [68° to 77° F]
  • for your protection, this bottle has an imprinted white seal with black printing “TAMPER EVIDENT SEAL”
  • do not use if this seal is missing or broken
  • use before expiration date marked on bottle

Inactive ingredients

INACTIVE INGREDIENT SECTION

boric acid, sodium borate, sodium chloride

Questions?

OTC - QUESTIONS SECTION

☎ Call 1-800-835-2263

Package Label.Principal Display Panel drug facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug Facts LabelDrug Facts Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1151101water 98.3 % Ophthalmic Irrigation SolutionPSN1
1151101water 983 MG/ML Ophthalmic Irrigation SolutionSCD1
1151101water 98.3 % Ophthalmic Irrigation SolutionSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0924-0163-01Physicians Care Eyewash29 mL in 1 BOTTLE, UNIT-DOSESOLUTION291
0924-0163-04Physicians Care Eyewash118 mL in 1 BOTTLE, UNIT-DOSESOLUTION1181
0924-0163-08Physicians Care Eyewash236 mL in 1 BOTTLE, UNIT-DOSESOLUTION2361
0924-0163-16Physicians Care Eyewash473 mL in 1 BOTTLE, UNIT-DOSESOLUTION4731
0924-0163-32Physicians Care Eyewash946 mL in 1 BOTTLE, UNIT-DOSESOLUTION9461

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0924-01630924-0163-16, 0924-0163-32, 0924-0163-08, 0924-0163-04, 0924-0163-01
87024-100

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
BORIC ACIDR57ZHV85D4IACT
SODIUM BORATE91MBZ8H3QOIACT
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
Physicians Care EyewashEYEWASHAcme United Corporation3e239b12-9a75-339d-e063-6294a90a72ae2025-09-06WarningsExact identifier
ndc (package): 0924-0163-04
ndc (package): 0924-0163-16
ndc (package): 0924-0163-01
ndc (package): 0924-0163-32
ndc (package): 0924-0163-08
ndc (product): 0924-0163
ndc11 (package): 00924016304
ndc11 (package): 00924016308
ndc11 (package): 00924016316
ndc11 (package): 00924016332
ndc11 (package): 00924016301
spl id: 3e238515-002f-f2f3-e063-6294a90a957a
spl set id: 3e239b12-9a75-339d-e063-6294a90a72ae

Reported adverse events (FAERS/openFDA)#

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