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Class II · ModerateActive recall

Rohto Dry-Aid

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot #: 4G1V, Exp 2027/06; 4J1V, 512VB 2027/09; 5D1V, 2028/03; 5G1V, 512VB 2028/06; 512V, 512VB 2028/08
Where it was soldNationwide within the United States
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Lack of Assurance of Sterility

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in Vietnam
Brand nameROHTO DRY-AID
Generic namePOVIDONE, PROPYLENE GLYCOL
Active ingredient(s)POVIDONE, UNSPECIFIED, PROPYLENE GLYCOL
Distributed by / forThe Mentholatum Company, Orchard Park, NY 14127
NDC10742-8162-2
Show the full FDA record
Full product labelRohto Cooling Eye Drops Dry Aid (povidone 0.68%, propylene glycol 0.3%), Sterile, TWIN PACK 0.34 FL OZ (10 mL) each, Distributed by: The Mentholatum Company, Orchard Park, NY 14127, Made in Vietnam, UPC 310742011159, NDC 10742-8162-2
Recalling firmRohto-Mentholatum (Vietnam) Co., Ltd.
DistributionNationwide within the United States
Quantity353 cartons
Recall initiated2026-07-14
Report date2026-07-29
Recall completed—
Recall numberD-0721-2026
ClassificationClass II
FDA statusOngoing
Origin on fileHo Chi Minh N/A Vietnam

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.