Label: QUALITY CHOICE EYE WASH- water solution/ drops
- NDC Code(s): 83324-192-04
- Packager: Chain Drug Marketing Assoc., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 30, 2025
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
- if you have open wounds in or near the eyes, and get medical help right away
- if solution changes color or becomes cloudy
When using this product
- remove contact lenses before using
- do not touch tip of container to any surface to avoid contamination
- replace cap after use
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Directions
For use with nozzle applicator.
- flush the affected eye(s) as needed
- control the rate of flow of solution by pressure on the bottle
- do not touch dropper tip to eye
When using an eye cup
- rinse the cup with Eye Wash immediately before each use
- avoid contamination of the rim and inside surfaces of the cup
- fill the cup half full with Eye Wash Solution and apply the cup to the affected eye(s), pressing tightly to prevent spillage
- tilt the head backward. Open eyelids wide and rotate eyeball to thoroughly wash the eye
- rinse cup with clean water after each use
- replace cap after use
- Other information
- Inactive ingredients
- Quality Choice Eye Wash 118 mL
-
INGREDIENTS AND APPEARANCE
QUALITY CHOICE EYE WASH
water solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-192 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 99.05 g in 100 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) SODIUM CHLORIDE (UNII: 451W47IQ8X) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM BORATE (UNII: 91MBZ8H3QO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-192-04 1 in 1 BOX 08/15/2024 1 118 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M018 08/15/2024 Labeler - Chain Drug Marketing Assoc., Inc. (011920774) Registrant - K.C. Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Inc. 114406598 manufacture(83324-192) Establishment Name Address ID/FEI Business Operations K.C. Pharmaceuticals, Inc. 174450460 pack(83324-192) , label(83324-192)

