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

Vicks Children's Botanicals Liquid Daytime/Nighttime Combo recalled

The Procter & Gamble is recalling Vicks Children's Botanicals Liquid Daytime/Nighttime Combo Pack plastic, 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: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Lot Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Product Number: 80338569, 80365757 Item UPC: 323900041073 Case UPC: 10323900041070 Expiration Dates: 0240C60405 07/31/2022, 0314C60402 10/31/2022, 11664334R2 - 05/31/2023, 11664334R3 - 05/31/2023, 11664334R4 - 05/31/2023, 11664334R5 - 05/31/2023, 11664334E1 - 05/31/2023, 12164334E1 07/31/2023, 12164334E2 - 07/31/2023, 12164334Y1 - 07/31/2023, 12164334Y2 - 07/31/2023, 12164334Y3 - 07/31/2023, 12164334Y4 - 07/31/2023, 12164334Y5 - 07/31/2023, 12164334Y6 - 07/31/2023, 12184334E1 - 07/31/2023, 12184334E2 - 07/31/2023, 12184334E3 - 07/31/2023, 12184334E4 - 07/31/2023, 12184334Y1 - 07/31/2023, 12184334Y2 - 07/31/2023, 12184334Y3 - 07/31/2023, 12184334Y4 - 07/31/2023, 12374334D1 - 07/31/2023, 12374334D2 - 07/31/2023, 12374334E0 - 07/31/2023, 12374334E1 - 07/31/2023, 12374334E2 - 07/31/2023, 12374334E3 - 07/31/2023, 12374334E4 - 07/31/2023, 12374334E5 - 07/31/2023, 12374334E6 - 07/31/2023, 12374334E7 - 07/31/2023, 12374334E8 - 07/31/2023, 12374334E9 - 07/31/2023, 12374334EA - 07/31/2023, 12374334Y1 - 07/31/2023, 12374334Y2 - 07/31/2023, 13214334D1 10/31/2023, 13214334D2 - 10/31/2023, 13214334J1 - 10/31/2023, 13214334K0 - 10/31/2023, 13214334K1 - 10/31/2023, 13214334K2 - 10/31/2023, 13214334K3 - 10/31/2023, 13214334K4 - 10/31/2023, 13214334K5 - 10/31/2023, 13214334K6 - 10/31/2023, 13214334K7 - 10/31/2023, 13214334K8 - 10/31/2023, 13214334K9 - 10/31/2023, 13214334P1 - 10/31/2023, 13214334P2 - 10/31/2023, 13624334S1 10/31/2023, 20124334E1 12/31/2023, 20124334E2 - 12/31/2023, 20124334E3 - 12/31/2023, 20124334K1 - 12/31/2023, 20124334K2 - 12/31/2023, 20124334K3 - 12/31/2023, 20124334K4 - 12/31/2023, 20384334E1 01/31/2024, 20384334E2 01/31/2024, 20384334E3 10/31/2024
Quantity recalled82,433 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-1533-2022
FDA event ID
90615
Recalling firm
The Procter & Gamble, Cincinnati, OH
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 2022Recall initiated by company
3 Aug 2022Classified by FDA+22 days
10 Aug 2022Published 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 Daytime/Nighttime Combo Pack 4oz plastic bottles

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.

AlaskaAlabamaArkansasArizonaCaliforniaColoradoConnecticutDelawareFloridaGeorgiaHawaiiIowaIdahoIllinoisIndianaKansasKentuckyLouisianaMassachusettsMaryland

Questions about this recall

Why was it recalled?

Acidified/Low Acid dietary supplement with no approved process.

Which lots are affected?

Batch Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Lot Numbers: 0240C60405, 0314C60402, 11664334R1, 11664334R2, 11664334R3, 11664334R4, 11664334R5, 11664334E1, 12164334E1, 12164334E2, 12164334Y1, 12164334Y2, 12164334Y3, 12164334Y4, 12164334Y5, 12164334Y6, 12184334E1, 12184334E2, 12184334E3, 12184334E4, 12184334Y1, 12184334Y2, 12184334Y3, 12184334Y4, 12374334D1, 12374334D2, 12374334E0, 12374334E1, 12374334E2, 12374334E3, 12374334E4, 12374334E5, 12374334E6, 12374334E7, 12374334E8, 12374334E9, 12374334EA, 12374334Y1, 12374334Y2, 13214334D1, 13214334D2, 13214334J1, 13214334K0, 13214334K1, 13214334K2, 13214334K3, 13214334K4, 13214334K5, 13214334K6, 13214334K7, 13214334K8, 13214334K9, 13214334P1, 13214334P2, 13624334S1, 20124334E1, 20124334E2, 20124334E3, 20124334K1, 20124334K2, 20124334K3, 20124334K4, 20384334E1, 20384334E2, 20384334E3 Product Number: 80338569, 80365757 Item UPC: 323900041073 Case UPC: 10323900041070 Expiration Dates: 0240C60405 07/31/2022, 0314C60402 10/31/2022, 11664334R2 - 05/31/2023, 11664334R3 - 05/31/2023, 11664334R4 - 05/31/2023, 11664334R5 - 05/31/2023, 11664334E1 - 05/31/2023, 12164334E1 07/31/2023, 12164334E2 - 07/31/2023, 12164334Y1 - 07/31/2023, 12164334Y2 - 07/31/2023, 12164334Y3 - 07/31/2023, 12164334Y4 - 07/31/2023, 12164334Y5 - 07/31/2023, 12164334Y6 - 07/31/2023, 12184334E1 - 07/31/2023, 12184334E2 - 07/31/2023, 12184334E3 - 07/31/2023, 12184334E4 - 07/31/2023, 12184334Y1 - 07/31/2023, 12184334Y2 - 07/31/2023, 12184334Y3 - 07/31/2023, 12184334Y4 - 07/31/2023, 12374334D1 - 07/31/2023, 12374334D2 - 07/31/2023, 12374334E0 - 07/31/2023, 12374334E1 - 07/31/2023, 12374334E2 - 07/31/2023, 12374334E3 - 07/31/2023, 12374334E4 - 07/31/2023, 12374334E5 - 07/31/2023, 12374334E6 - 07/31/2023, 12374334E7 - 07/31/2023, 12374334E8 - 07/31/2023, 12374334E9 - 07/31/2023, 12374334EA - 07/31/2023, 12374334Y1 - 07/31/2023, 12374334Y2 - 07/31/2023, 13214334D1 10/31/2023, 13214334D2 - 10/31/2023, 13214334J1 - 10/31/2023, 13214334K0 - 10/31/2023, 13214334K1 - 10/31/2023, 13214334K2 - 10/31/2023, 13214334K3 - 10/31/2023, 13214334K4 - 10/31/2023, 13214334K5 - 10/31/2023, 13214334K6 - 10/31/2023, 13214334K7 - 10/31/2023, 13214334K8 - 10/31/2023, 13214334K9 - 10/31/2023, 13214334P1 - 10/31/2023, 13214334P2 - 10/31/2023, 13624334S1 10/31/2023, 20124334E1 12/31/2023, 20124334E2 - 12/31/2023, 20124334E3 - 12/31/2023, 20124334K1 - 12/31/2023, 20124334K2 - 12/31/2023, 20124334K3 - 12/31/2023, 20124334K4 - 12/31/2023, 20384334E1 01/31/2024, 20384334E2 01/31/2024, 20384334E3 10/31/2024

Where was it 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 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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 90615

This product is part of a recall event; the main page for the event is Vicks Children's Botanicals Liquid Nighttime plastic recalled.

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