PHYSICIANS CARE EYEWASH- eyewash solution

Physicians Care Eyewash by

Drug Labeling and Warnings

Physicians Care Eyewash by is a Otc medication manufactured, distributed, or labeled by Acme United Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Purified water 98.3%

Purpose

Eyewash

Warnings

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

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

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

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• 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

• 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

boric acid, sodium borate, sodium chloride

Questions?

☎ Call 1-800-835-2263

Package Label.Principal Display Panel drug facts

INGREDIENTS AND APPEARANCE

PHYSICIANS CARE EYEWASH 
eyewash solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0924-0163(NDC:87024-100)
Route of Administration	OPHTHALMIC

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R)	WATER	465 mL  in 473 mL

Inactive Ingredients
Ingredient Name	Strength
BORIC ACID (UNII: R57ZHV85D4)
SODIUM BORATE (UNII: 91MBZ8H3QO)
SODIUM CHLORIDE (UNII: 451W47IQ8X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0924-0163-16	473 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/29/2025
2	NDC: 0924-0163-32	946 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/29/2025
3	NDC: 0924-0163-08	236 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/29/2025
4	NDC: 0924-0163-04	118 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/29/2025
5	NDC: 0924-0163-01	29 mL in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product	09/29/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	09/29/2025

Labeler - Acme United Corporation (001180207)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		045924339	relabel(0924-0163) , repack(0924-0163)

Establishment
Name	Address	ID/FEI	Business Operations
Acme United Corporation		080119599	relabel(0924-0163) , repack(0924-0163)