# FDA recall D-1173-2023

> **Vi-Jon, LLC** · Class III · drug recall initiated 2023-09-05.

## 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.

## Distribution

The consignee list includes one distributor with seven distribution centers. No product was sold under government contract. No product was sold to any federal, state, or local agency in the school lunch program.

## Key facts

- **Recall number:** D-1173-2023
- **Recalling firm:** Vi-Jon, LLC
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2023-09-05
- **Report date:** 2023-09-27
- **Termination date:** 2025-01-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Smyrna, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1173-2023

## Citation

> AI Analytics. FDA recall D-1173-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/D-1173-2023. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
