Recent Update
Active Recall
FDA Safety Communication
FDA Warning Letter
FDA Untitled Letter
Manufacturing Violations
Frankenstein Eye Drop
Non-Compliant Ingredients
Prescription Drug Claims
FDA Inspection OAI
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Learn more about 12/3/24 recall: https://www.biologiceyedrops.org/watch/regener-eyes-recall
Brand:Regener-Eyes
Country of Manufacture:USA
Package Type:Multi-dose PF bottle
Contains preservative(s):No
Active ingredient(s):Glycerin 0.4%
Inactive ingredient(s):Sodium chloride, water
NDC(s):82305-006-01
FDA Action:10/5/22 Untitled Letter to Regener-Eyes LLC
4/10/23 Public Safety Notification on Amniotic Fluid Eyedrops
8/16/24 Warning Letter to Regenerative Processing Plant LLC
4/10/23 Public Safety Notification on Amniotic Fluid Eyedrops
8/16/24 Warning Letter to Regenerative Processing Plant LLC
Last updated:12-06-24