CLASS II Food recall · Reported 10 Aug 2022 · FDA Enforcement Report

Vicks Children's Botanicals Liquid Nighttime recalled

The Procter & Gamble is recalling Vicks Children's Botanicals Liquid Nighttime, distributed in 45 states. The recall was initiated on 12 Jul 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBatch 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

Quantity recalled18,490 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-1535-2022
FDA event ID: 90615
Recalling firm: The Procter & Gamble, Cincinnati, OH
Brand: Vicks Children's
Classification: Class II
Status: Terminated
Recall initiated: 12 Jul 2022
FDA classified: 3 Aug 2022
Reported: 10 Aug 2022
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Foreign Material
Product category: Other

Timeline

12 Jul 2022	Recall initiated by company
3 Aug 2022	Classified by FDA	+22 days
10 Aug 2022	Published in enforcement report	+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Acidified/Low Acid dietary supplement with no approved process.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Vicks Children's Botanicals Liquid Nighttime 4oz plastic bottle

Where it was distributed

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.

Alaska Alabama Arkansas Arizona California Colorado Connecticut Delaware Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kansas Kentucky Louisiana Massachusetts Maryland

Questions about this recall

Is Vicks Children's Botanicals Liquid Nighttime recalled?

Yes. The Procter & Gamble recalled Vicks Children's Botanicals Liquid Nighttime on 12 Jul 2022. The recall is Class II and its status is Terminated. Recall number F-1535-2022.

Why was it recalled?

Acidified/Low Acid dietary supplement with no approved process.

Which lots are affected?

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

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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