CLASS I Drug recall · Reported 28 Feb 2024 · FDA Enforcement Report
TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid recalled
Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare is recalling TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, distributed nationwide in the US. The recall was initiated on 1 Feb 2024 and the FDA has classified it as Class I.
Check your package
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
Recall details
- Recall number
- D-0346-2024
- FDA event ID
- 93928
- Recalling firm
- Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare, Tarrytown, NY
- Classification
- Class I
- Status
- Completed
- Recall initiated
- 1 Feb 2024
- FDA classified
- 22 Feb 2024
- Reported
- 28 Feb 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Benzene
Timeline
| 1 Feb 2024 | Recall initiated by company | |
| 22 Feb 2024 | Classified by FDA | +21 days |
| 28 Feb 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Chemical Contamination; presence of benzene.
Product as listed by the FDA
TING 1% Tolnaftate Athlete's Foot Spray Antifungal Spray Liquid, NET WT 4.5 oz. (128 g) cans, Distributed by: Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company, Tarrytown, NY 10591 UPC 3 63736 81961 3
Where it was distributed
Product was distributed nationwide and to 4 foreign accounts. Guaynabo, Puerto Rico; Georgetown, Guyana; Baghdad, Iraq; Accra, Ghana.
Questions about this recall
Why was it recalled?
Chemical Contamination; presence of benzene.
Which lots are affected?
Lot # 0H50545, Exp. date 07/31/24; 1G50645, Exp. date 06/30/25
Where was it sold?
Product was distributed nationwide and to 4 foreign accounts. Guaynabo, Puerto Rico; Georgetown, Guyana; Baghdad, Iraq; Accra, Ghana.
What should I do if I have it?
Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
More recalls from Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS I | Americaine, (benzocaine 20%) Benzocaine Topical Anesthetic recalledAmericaine | Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare | Benzene | Nationwide |