Label: ADVANCED EYE RELIEF EYE WASH- water solution solution/ drops
- NDC Code(s): 24208-005-04
- Packager: Bausch & Lomb Incorporated
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 17, 2025
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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
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
- Keep out of reach of children.
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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
[image eye] Without Eye Cup
[image eye] With Eye CupWhen using an eye cup
- rinse the cup with Bausch + Lomb Advanced Eye Relief ®Eye Wash solution immediately before each use
- avoid contamination of the rim and inside surfaces of the cup
- fill the cup half full with Bausch + Lomb Advanced Eye Relief ®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
- Questions or comments?
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INGREDIENTS AND APPEARANCE
ADVANCED EYE RELIEF EYE WASH
water solution solution/ dropsProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24208-005 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) BENZALKONIUM (UNII: 7N6JUD5X6Y) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24208-005-04 1 in 1 CARTON 02/02/2017 1 118 mL in 1 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 02/02/2017 Labeler - Bausch & Lomb Incorporated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 114406598 manufacture(24208-005)
