FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Vicks ZzzQuil Liquid Melatonin Syrup Adult 8oz plastic bott…
- Published
- August 10, 2022
- Distribution
- Alaska, Alabama, Arkansas, Arizona, Cali…
The Procter & Gamble Company Recall: Acidified/Low Acid dietary supplement with no approved process.
United States
TerminatedClass II
- Company
- The Procter & Gamble Company
- Product
- Vicks Children's Botanicals Liquid Daytime 4oz plastic bott…
- Recall date
- July 12, 2022
- Terminated
- August 15, 2024
- Source
- FDA
Reason for recall
Acidified/Low Acid dietary supplement with no approved process.
- - Recall initiated
- - Reported by source
- - Recall terminated
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle | Not published in this source record | 34,526 cases | 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
- 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.
Official source record
- Agency
- FDA
- Dataset
- FDA Food Enforcement (Recalls)
- Recall number
- F-1534-2022
- Event ID
- 90615
- Status
- Terminated
- Classification
- Class II
- Company
- The Procter & Gamble Company
- Product description
- Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
- Quantity
- 34,526 cases
- Reason
- Acidified/Low Acid dietary supplement with no approved process.
- Recall initiation date
- July 12, 2022
- Report date
- August 10, 2022
- Classification date
- Not published in this source record
- Termination date
- August 15, 2024
- Distribution pattern
- 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.
- UPC, lot, and code information
- 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
- Voluntary or mandated
- Voluntary: Firm initiated
- Initial notification method
- Source last updated
- Not tracked separately from the Public Health Trace retrieval date below
- Public Health Trace retrieval date
Other products recalled under this same event
This recall shares FDA event ID 90615 with 4 other product entries in Public Health Trace.
FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Vicks ZzzQuil Liquid Melatonin Syrup Pediatric 8oz plastic…
- Published
- August 10, 2022
- Distribution
- Alaska, Alabama, Arkansas, Arizona, Cali…
FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Vicks Children's Botanicals Liquid Nighttime 4oz plastic bo…
- Published
- August 10, 2022
- Distribution
- Alaska, Alabama, Arkansas, Arizona, Cali…
FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Vicks Children's Botanicals Liquid Daytime/Nighttime Combo P…
- Published
- August 10, 2022
- Distribution
- Alaska, Alabama, Arkansas, Arizona, Cali…
Responsible company: The Procter & Gamble Company
Other recalls from The Procter & Gamble Company
FDA Recall United States Terminated Historical recordClass II
The Procter & Gamble Company
- Product
- Meta Psyllium Fiber Capsules packaged as 100 count or 160 co…
- Published
- February 28, 2024
- Distribution
- Alabama, Arizona, Arkansas, California,…
FDA Recall Terminated Historical recordClass II
Secret Dry Spray, Aluminum chlorohydrate 23.5%, Antiperspirant, Rose, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-380-10, UPC 0 37000 79884 2
- Published
- January 24, 2024
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Secret, Dry Spray, (Aluminum chlorohydrate 23.5%), Antiperspirant, Lavender, Topical spray can Net Wt 3.8 oz (107 g), Dist. by: Procter & Gamble, Cincinnati, OH 45202. NDC: 69423-383-10, UPC: 0 37000 72986 0
- Published
- January 24, 2024
- Distribution
- Nationwide
Where this information comes from
View FDA enforcement record -- the specific openFDA record this summary was built from.
No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
Technical source data
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
Frequently asked questions
What does a Class II mean?
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
Is this recall still active?
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
What should I do if I have this product?
Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.
Where can I find more official information?
The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.
This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.
