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Class II: temporary or reversible health riskTerminated

The Procter & Gamble Vicks Children's Botanicals Liquid Daytime Recall

Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle

The Procter & Gamble Company · Cincinnati, OH

Risk level
Class II
Reported by FDA
Aug 10, 2022
Recall ID
F-1534-2022
Check your lot numberHow we source this data

Summary

The Procter & Gamble recalled Vicks Children's Botanicals Liquid Daytime starting Jul 12, 2022. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1534-2022 on Aug 10, 2022. Reason: Acidified/Low Acid dietary supplement with no approved process. Status: Terminated.

Why it was recalled

Acidified/Low Acid dietary supplement with no approved process.

Product description

Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle

Lot numbers, UPCs & expiration codes

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

Where it was sold

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.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1534-2022
Classification
Class II
Status
Terminated
Recall initiated
Jul 12, 2022
FDA report date
Aug 10, 2022
Quantity
34,526 cases
Recall type
Voluntary: Firm initiated
Recalling firm
The Procter & Gamble Company

Original FDA data

Every field from FDA enforcement report F-1534-2022, exactly as published.

Show all FDA fields
City
Cincinnati
State
OH
Status
Terminated
Country
United States
Event ID
90615
Address
1 Procter And Gamble Plz
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
Postal code
45202-3315
Report date
Aug 10, 2022
Product type
Food
Recall number
F-1534-2022
Classification
Class II
Recalling firm
The Procter & Gamble Company
Product quantity
34,526 cases
Termination date
Aug 15, 2024
Reason for recall
Acidified/Low Acid dietary supplement with no approved process.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
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.
Recall initiation date
Jul 12, 2022
Initial firm notification
E-Mail
Center classification date
Aug 3, 2022

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1534-2022, published Aug 10, 2022. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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