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PhysiciansCare Ophthalmic Solution Eyewash

Dosage form: solution
Ingredients: WATER 929g in 946mL
Labeler: Acme United Corporation
NDC Code: 0924-0160

PhysiciansCare Ophthalmic Solution Eyewash

Active Ingredients

Purified Water 98.3%

Purpose

Eyewash


Use

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

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 

Stop use and ask a doctor if you experience

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

 

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

 

Directions

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

PHYSICIANSCARE OPHTHALMIC SOLUTION EYEWASH 
purified water 98.3% solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0160(NDC:65785-160)
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
WATER (WATER) WATER929 g  in 946 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID 
SODIUM BORATE 
SODIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:0924-0160-0130 mL in 1 BOTTLE, UNIT-DOSE
2NDC:0924-0160-04118 mL in 1 BOTTLE, UNIT-DOSE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02230506/24/2013
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIOperations
Acme United Corporation045924339relabel(0924-0160), repack(0924-0160)
Establishment
NameAddressID/FEIOperations
Acme United Corporation Pac-Kit Safety Division883538258relabel(0924-0160), repack(0924-0160)

 
Acme United Corporation

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Medically reviewed on Jun 25, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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