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(Reuters) - The U.S. Food and Drug Administration (FDA) on Wednesday warned consumers not to use unapproved eye drops that closely resemble Bausch + Lomb's Lumify product for redness relief.
According to the FDA, consumers can easily mistake the copycat products for Bausch + Lomb’s Lumify brand eye drops. The FDA says the packaging for South Moon, Rebright and FivFivGo products look ...
The agency said in an announcement Wednesday that these unapproved copycat products can be easily mistaken for Bausch + Lomb’s Lumify drops, which are approved to ease eye redness.
LightEyez MSM Eye Drops-Eye Repair, NDC number not provided. CVS Health Lubricant Eye Drops 15 ml (single pack) , NDC number 76168-702-15. CVS Health Lubricant Eye Drops 15 ml (twin pack) , NDC ...
Eye drops are being recalled due to a rare bacterium found in artificial tears. Find a list of recalled drops in 2023. Plus, eye infection symptoms.
Bausch & Lomb (since 2010 stylized as Bausch + Lomb[2]) is an American-Canadian eye health products company based in Vaughan, Ontario, Canada. It is one of the world's largest suppliers of contact lenses, [3] lens care products, pharmaceuticals, intraocular lenses, and other eye surgery products. [4][5] The company was founded in Rochester, New ...
ReNu is a brand of soft contact lens care products produced by Bausch & Lomb. [1] By far the most popular brand of lens solutions until 2006, ReNu has rebranded its formulations as renu sensitive (formerly ReNu Multi-Purpose) and renu fresh (formerly ReNu MultiPlus), the latter containing a patented ingredient called hydranate, known by chemists as hydroxyalkylphosphonate, that removes protein ...
The agency said due to this, Dr Berne “verbally agreed” on 21 August 21 to “voluntary recall” the Dr Berne’s MSM Drops 5 per cent Solution. The FDA said it emailed LightEyez Limited to ...