EYEWASH STATION ADDITIVE CONCENTRATE- chlorhexidine gluconate and propylene glycol liquid 
Acme United Corporation

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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PhysiciansCare Eyewash Station Additive Concentrate

Product Information

Ingredients

Chlorhexidine gluconate 1% w/v Purified Water, Propylene Glycol

Purpose

Preservative

Use

A preservative for use in potable self-contained emergency eyewash stations

Warnings

For external use only. In case of contact with eye in undiluted form, flush with clean water

Do not use

  • in full strength

When using this product

  • do not change dilution or use with other chemicals
  • do not reuse

Stop use and ask a doctor if you have

  • 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

Other information

Questions ?

☎ Call 1.800.835.2263

Bottle Label Bottle Label

EYEWASH STATION ADDITIVE CONCENTRATE 
chlorhexidine gluconate and propylene glycol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0159(NDC:65785-035)
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE145.6 kg  in 2800 L
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL280 kg  in 2800 L
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 2374.4 L  in 2800 L
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0924-0159-080.236 L in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/09/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34901/09/2023
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-0159) , repack(0924-0159)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599repack(0924-0159) , relabel(0924-0159)

Revised: 1/2023
Document Id: f19fbe45-b7a7-ddc1-e053-2a95a90abd3b
Set id: f19fbe28-b928-7c6e-e053-2995a90a43cb
Version: 1
Effective Time: 20230106
 
Acme United Corporation