Label: LEADER EYE WASH- purified water solution
- NDC Code(s): 70000-0018-1
- Packager: Cardinal Health
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 2023
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- 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 Solution 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 affected eye(s), pressing tightly to prevent spillage
- tilt the head backward. Open eyelids wide and rotate eyeballs to thoroughly wash the eye
- rinse cup with clean water after each use
- replace cap after use
- Other information
- Inactive ingredients
- Questions or comments?
- Leader Eye Wash
-
INGREDIENTS AND APPEARANCE
LEADER EYE WASH
purified water solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0018 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) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0018-1 1 in 1 BOX 07/09/2019 1 118 mL in 1 BOTTLE, DROPPER; 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 07/09/2019 Labeler - Cardinal Health (063997360) Registrant - KC Pharmaceuticals, Inc. (174450460) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorperated 114406598 manufacture(70000-0018) Establishment Name Address ID/FEI Business Operations KC Pharmaceuticals, Inc. 174450460 pack(70000-0018) , label(70000-0018)