Recall archive / FDA food enforcement
Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle — FDA record F-1535-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 12, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle
- Reason
- Acidified/Low Acid dietary supplement with no approved process.
- Classification
- Class II
- Recalling firm
- The Procter & Gamble Company
- Quantity
- 18,490 cases
- Agency-reported status
- Terminated
- Source record identifier
- F-1535-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Batch Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401,1321C60402, 1321C604Q1, 2038C60401, 2152C60401 , 2153C60401 Lot Numbers: 0240C60404, 1166C60401, 1218C60401, 1237C60401, 1321C60401, 1321C60402, 1321C604Q1, 2038C60401, 2152C60401, 2153C60401 Product Number: 80338364 Item UPC: 323900041066 Case UPC: 10323900041063 Expiration Dates: 0240C60404 07/31/2022, 1166C60401 05/31/2023, 1218C60401 07/31/2023, 1237C60401 07/31/2023, 1321C60401 10/31/2023, 1321C60402 10/31/2023, 1321C604Q1 10/31/2023, 2038C60401 01/31/2024, 2152C60401 05/31/2024, 2153C60401 05/31/2024 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Alaska, Alabama, Arkansas, Arizona, California, Colorado, Connecticut, Delaware, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Maine, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, North Dakota, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and West Virginia.
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- North Carolina
- North Dakota
- New Hampshire
- New Jersey
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Washington
- Wisconsin
- West Virginia
Dates in the source
- Report date
- Aug 10, 2022
- Recall initiation date
- Jul 12, 2022
- Center classification date
- Aug 3, 2022
- Termination date
- Aug 15, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.