Procter & Gamble recalls Crest 3D White Advanced Triple Whitening toothpaste due to missing label indicating a different formulation. Consumers should check product details and contact the company for guidance.
Labeling: Missing label: the product tube was missing a label and contained a different formulation.
Procter & Gamble is recalling Crest 3D White Fluoride Anticavity Toothpaste with a missing label that shows it contains a different formulation than advertised. This could lead to confusion about the product's actual contents.
The product tube was missing a label, which means consumers might not know it contains a different formulation than what was advertised. This could lead to confusion about the product's intended use and potential effects.
Crest 3D White Advanced Triple Whitening toothpaste users who purchased the product between specific dates. Those who used the product without noticing the missing label may be at risk of using an unintended formulation.
Check for the missing label on the tube. The product has a specific UPC code: 037000171867 for the 5-count bundle and 0 37000 598534 for the individual carton.
Look for the missing label on the tube to confirm if it's the recalled product.
The product tube was missing a label, which means it contains a different formulation than advertised.
Check for the missing label on the tube. The product has specific UPC codes: 037000171867 for the 5-count bundle and 0 37000 598534 for the individual carton.
The official recall notice does not specify a remedy, so contact Procter & Gamble for guidance.
We’ve drafted a message you can send Procter & Gamble to request your refund or repair — edit it as you like.
Subject: Recall D-1290-2022 — Procter & Gamble Procter & Gamble Hello, I own a Procter & Gamble that is covered by recall D-1290-2022 from Procter & Gamble. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
