- Active ingredient
- Purpose
- Uses
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Warnings
Do not use if solution changes color or becomes cloudy
When using this product
- •
- remove contact lenses before use
- •
- do not touch tip of container to any surface to avoid contamination
- •
- replace cap after use
Stop use and ask a doctor if
- •
- you experience eye pain, changes in vision, continued redness or irritation of the eye
- •
- condition worsens or persists
- •
- you have open wounds in or near the eye
- Keep out of reach of children.
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Directions
- •
- flush the affected eye(s) as needed
- •
- control the rate of flow of solution by placing pressure on the bottle
When using an eye cup
- •
- rinse the cup with clean water immediately before each use
- •
- avoid contamination of the rim and inside surfaces of the cup
- •
- fill the cup half full and apply the cup to the affected eye(s), pressing tightly to prevent the escape of the liquid
- •
- tilt the head backward. Open eyelid wide and rotate eyeball to ensure thorough bathing with the wash
- •
- rinse the cup with clean water after each use
- Other information
- Inactive ingredients
- Questions or comments?
- HOW SUPPLIED
- Purified Water
-
INGREDIENTS AND APPEARANCE
EYE IRRIGATING
purified water solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50090-0382(NDC:0536-0901) Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength WATER (UNII: 059QF0KO0R) (WATER - UNII:059QF0KO0R) WATER 99.05 mL in 100 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) EDETATE DISODIUM (UNII: 7FLD91C86K) SORBIC ACID (UNII: X045WJ989B) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50090-0382-0 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/28/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date Unapproved drug other 10/07/2011 Labeler - A-S Medication Solutions (830016429) Establishment Name Address ID/FEI Business Operations A-S Medication Solutions 830016429 RELABEL(50090-0382)