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Lower risk Drug recall · FDA · Published July 8, 2022

Crest 3D White Toothpaste Recall: Missing Label Causes Different Formulation

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.

🇺🇸 FDA recall #D-1290-2022DrugProcter & Gamble ›
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Contact the company

Recalling firmThe Procter & Gamble Company1 Procter And Gamble Plz · Cincinnati, OH 45202-3315
✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/34436-crest-3d-white-toothpaste-recall-missing-label-causes-different-formulation.

Source Summary by GovInfoNow · govinfonow.com/recall/34436-crest-3d-white-toothpaste-recall-missing-label-causes-different-formulation · Updated August 18, 2026 · FDA enforcement record: FDA #D-1290-2022

Cite this page

“Crest 3D White Toothpaste Recall: Missing Label Causes Different Formulation.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/34436-crest-3d-white-toothpaste-recall-missing-label-causes-different-formulation. Based on FDA recall #D-1290-2022 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1290-2022%22&limit=1).

The Food and Drug Administration announced on July 8, 2022, that The Procter & Gamble Company is recalling Crest 3D White Fluoride Anticavity Toothpaste because the product tube was missing a label and contained a different formulation. Owners should stop using the product immediately.

How to tell if you have it

  • Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening
  • 0.243% sodium fluoride
  • Net Wt. 5.6 oz (158 g)
  • UPC 0 37000 598534
  • 5-count Bundle UPC 037000171867
  • Lot 13191707B4, Exp. 10/31/2023
  • Lot 13511707Y1, Exp. 10/31/2023

The hazard

The recalled Crest 3D White Fluoride Anticavity Toothpaste tubes were missing labels and contained a different formulation than intended. The FDA classified this labeling error as a Class III recall.

Context

GovInfoNow's records show The Procter & Gamble Company has four other recalls on record since November 23, 2021. Recent brand recalls include Procter & Gamble Meta Psyllium Fiber Capsules (February 1, 2024) and Vicks ZzzQuil Liquid Melatonin Syrup (July 12, 2022). Other recent recalls of similar products include American Regent Levocarnitine Injection (April 16, 2026), ORL Kids Natural Toothpaste (December 8, 2025), and American Health Packaging Buprenorphine Tablets (August 19, 2026).

How to tell if you have this one

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.

  • Brand
    Procter & Gamble
  • Product
    Crest 3D White Fluoride Anticavity Toothpaste, Advanced Triple Whitening, 0.243% sodium fluoride, Net Wt. 5.6 oz (158
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the missing label on the tube to confirm if it's the recalled product.

Where it went and when

Where it was distributed

Distributed in Washington.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “Washington State” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Washington.

Recall timeline

FDA published this recall 26 days after the firm started it.

1. Firm started the recall: Jul 8, 202212. FDA classified it Class III: Jul 26, 202223. Published in FDA’s Enforcement Report: Aug 3, 202232022
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #D-1290-2022 (July 8, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1290-2022 to see it in context.
  • Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA