PHYSICIANSCARE EYEWASH STATION ADDITIVE CONCENTRATE- chlorhexidine gluconate and propylene glycol liquid solution 
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.

----------

PhysiciansCare Eyewash Station Additive Concentrate

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

When using this product

Stop use and ask a doctor ifyou have any of the following

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

Directions

Other information

Questions? Call 1-800-254-5050 9 a.m. to 5 p.m. EST Mon-Fri

Inactive Ingredients

Water

Eyewash Station Additive Concentrate 8 oz Label

PRINCIPAL DISPLAY PANEL - 236 mL Bottle Label

EYEWASH STATION ADDITIVE CONCENTRATE

NDC 0924-0169-08

A preservative for potable water.

Preserves from 5 - 20 US Gallons

(15 - 76 Liters)

FOR USE IN EMERGENCY

EYEWASH STATIONS

Acme United Corporation

55 Walls Drive

Fairfield, CT 06824

www.FirstAidOnly.com

8 Fl Oz [236mL]

PHYSICIANSCARE EYEWASH STATION ADDITIVE CONCENTRATE 
chlorhexidine gluconate and propylene glycol liquid solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0169
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL280 kg  in 2800 L
CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) (CHLORHEXIDINE - UNII:R4KO0DY52L) CHLORHEXIDINE GLUCONATE145.6 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:0924-0169-080.236 L in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product01/26/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34901/26/2016
Labeler - Acme United Corporation (001180207)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation045924339relabel(0924-0169) , repack(0924-0169)
Establishment
NameAddressID/FEIBusiness Operations
Acme United Corporation080119599repack(0924-0169) , relabel(0924-0169)
Establishment
NameAddressID/FEIBusiness Operations
Niagara Pharmaceuticals, Inc.205477792manufacture(0924-0169)

Revised: 11/2019
Document Id: 968aa925-85b3-7516-e053-2995a90a64e2
Set id: 2a3f0a3e-3ae2-4d7e-e054-00144ff88e88
Version: 4
Effective Time: 20191104
 
Acme United Corporation