Label: ADVANCED EYE RELIEF EYE WASH- water solution solution/ drops
- NDC Code(s): 24208-005-04
- Packager: Bausch & Lomb Incorprated
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated June 5, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- if you have open wounds in or near the eyes, and get medical help right away
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- if solution changes color or becomes cloudy
When using this product
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- remove contact lenses before using
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- do not touch tip of container to any surface to avoid contamination
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- replace cap after use
Stop use and ask a doctor if
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- you experience eye pain, changes in vision, continued redness or irritation of the eye
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- condition worsens or persists
- Keep out of reach of children.
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Directions
For use with nozzle applicator.
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- flush the affected eye(s) as needed
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- control the rate of flow of solution by pressure on the bottle
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- do not touch dropper tip to eye
[image eye] Without Eye Cup
[image eye] With Eye CupWhen using an eye cup
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- rinse the cup with Bausch + Lomb Advanced Eye Relief ® Eye Wash solution immediately before each use
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- avoid contamination of the rim and inside surfaces of the cup
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- 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
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- tilt the head backward. Open eyelids wide and rotate eyeball to thoroughly wash the eye
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- rinse cup with clean water after each use
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- replace cap after use
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel-Carton
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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 final part349 02/02/2017 Labeler - Bausch & Lomb Incorprated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 114406598 MANUFACTURE(24208-005)
