Kroger Mint Burst ANTISEPTIC MOUTH RINSE ANTIGINGIVITIS/ANTIPLAQUE — Class III drug recall D-1173-2023
Terminated recall by Vi-Jon, LLC, reported 2023-09-27. Incorrect/Undeclared Excipients.
| Recall number | D-1173-2023 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vi-Jon, LLC, Smyrna, TN, United States |
| Recall initiated | 2023-09-05 |
| Classified | 2023-09-21 |
| Reported by FDA | 2023-09-27 |
| Terminated | 2025-01-29 |
| Quantity | 245,904 bottles |
| Reason classes | undeclared allergen |
| UPC / GTIN / UDI-DI | 00011110380807 |
| Lot numbers | 0589344, 0589626, 0589678, 0594596, 0595970, 0597832, 0601219, 0601488, 0604129 |
| Expiration dates | 2025-01-02, 2025-03-08, 2025-04-13, 2025-04-30, 2025-05-16, 2025-06-26, 2025-07-18 |
Product
Kroger Mint Burst ANTISEPTIC MOUTH RINSE ANTIGINGIVITIS/ANTIPLAQUE (Eucalyptol 0.092%, menthol 0.042%, Methyl salicylate 0.06%, thymol 0.064%), packaged in 16.9 FL OZ (500 mL) bottle, DISTRIBUTED BY THEKROGER CO. CINCINNATI, OHIO 45202, UPC 011110380807
Reason for recall
Incorrect/Undeclared Excipients.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1173-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.