Label: EYEWASH ADDITIVE CONCENTRATE- water and propylene glycol liquid
- NDC Code(s): 66051-236-80
- Packager: Haws Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 31, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
- Warnings
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Directions
- wear protective eyewear and gloves
- clean potable eyewash station and rinse with potable water
- partially fill station with potable water
- remove tamper evident seal and cap of bottle
- add entire contents of the bottle to the eyewash station container
- fill the station to the manufacturer’s required level
- date and initial inspection tag
- station should be cleaned and refilled every 120 days when using this product
- in advance of emergency, add the concentrate to potable water to have a solution available
- Inactive ingredient
- Other information
- Questions ?
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PRINCIPAL DISPLAY PANEL
HAWS
NDC 66051-236-80
EYEWASH ADDITIVE CONCENTRATE
Algaecide, Bactericide, Fungicide
Antimicrobial preservative for a self-contained, emergency eyewash station.
Preserves from 5 - 20 US Gallons
(18.9 - 75.7 Liters)
Manufactured for
Haws Corporation Sparks NV 89431
www.hawsco.comModel 9082
Made in Canada
8 Fl Oz [236 mL]
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INGREDIENTS AND APPEARANCE
EYEWASH ADDITIVE CONCENTRATE
water and propylene glycol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66051-236 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 2374.4 L in 2800 L PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 280 kg in 2800 L Inactive Ingredients Ingredient Name Strength CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) 145.6 kg in 2800 L Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66051-236-80 0.236 L in 1 BOTTLE, UNIT-DOSE; Type 0: Not a Combination Product 07/02/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 07/02/2019 Labeler - Haws Corporation (009124785) Registrant - Haws Corporation (009124785) Establishment Name Address ID/FEI Business Operations Niagara Pharmaceuticals Inc. 205477792 manufacture(66051-236)