Children's Botanicals Daytime (P&G) – unapproved process (2022)
Class II: A situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Class II recall indicates potential for temporary health effects.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle
Brand
The Procter & Gamble Company
Lot Codes / Batch Numbers
Batch Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 2110C60401 Lot Numbers: 0240C60402, 0279C60401, 1176C60401, 1216C60403, 1237C60402, 1321C60404, 2012C60401, 2012C60402, 2012C60403, 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
Products Sold
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
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Daytime 4oz plastic bottle due to Acidified/Low Acid dietary supplement with no approved process.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Acidified/Low Acid dietary supplement with no approved process.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NV, NH, NJ, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WV, WI
Page updated: Jan 6, 2026