FDA recall record
Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of August 15, 2024. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
Reason
Acidified/Low Acid dietary supplement with no approved process.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
Code information listed by FDA
Batch Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 2110C60401 Lot Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 2110C60401 Product Number: 80338363 Item UPC: 323900041059 Case UPC: 10323900041056 Expiration Dates: 0240C60402 07/31/2022, 0279C60401 09/30/2022 , 1176C60401 05/31/2023, 1216C60403 07/31/2023, 1237C60402 07/31/2023, 1321C60404 10/31/2023, 2012C60401 12/31/2023, 2012C60402 12/31/2023, 2012C60403 12/31/2023, 2110C60401 03/31/2024
Distribution and firm information
Recalling firm listed by FDA: The Procter & Gamble Company
Firm location listed by FDA: Cincinnati, OH, United States
Distribution reported by FDA: 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.
Product quantity listed by FDA: 34,526 cases
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.