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Lower risk Drug recall · FDA · Published February 1, 2021

Scott Moisturizing Foam Hand Sanitizer Label Mix-Up Recall

Kimberly-Clark recalls Scott Moisturizing Foam Hand Sanitizer due to incorrect labeling with some bottles containing Foam Skin Cleanser soap.

🇺🇸 FDA recall #D-0319-2021DrugKimberly-Clark ›
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Recalling firmKimberly-Clark Corporation1400 Holcomb Bridge Rd · Roswell, GA 30076-2190
✎ GovInfoNow plain-language explainer

What happened, in plain English

Kimberly-Clark is recalling Scott Moistur: 1.2 liters of Moisturizing Foam Hand Sanitizer because some bottles are incorrectly labeled as hand sanitizer when they actually contain Foam Skin Cleanser soap. This mix-up could lead to confusion about what product is being used. Read more at govinfonow.com/recall/36538-scott-moisturizing-foam-hand-sanitizer-label-mix-up-recall.

Source Summary by GovInfoNow · govinfonow.com/recall/36538-scott-moisturizing-foam-hand-sanitizer-label-mix-up-recall · Updated October 4, 2026 · FDA enforcement record: FDA #D-0319-2021

Cite this page

“Scott Moisturizing Foam Hand Sanitizer Label Mix-Up Recall.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36538-scott-moisturizing-foam-hand-sanitizer-label-mix-up-recall. Based on FDA recall #D-0319-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0319-2021%22&limit=1).

Why it’s dangerous

The hazard involves a labeling mix-up where some bottles of Scott Moisturizing Foam Hand Sanitizer are incorrectly labeled as hand sanitizer when they actually contain Foam Skin Cleanser soap. This could cause confusion about which product is being used, potentially leading to improper use of the product.

Who’s affected

People who own or use Scott Moisturizing Foam Hand Sanitizer products in the U.S. or Canada are affected. Those most at risk are individuals who may have used the incorrectly labeled soap instead of hand sanitizer.

How to tell if you have this one

Check for Scott Moisturizing Foam Hand Sanitizer, 1.2 liters (40.5 fl oz) with UPC 0 36000 91592 1 or Product Code 91590. The product was distributed in the U.S. by Kimberly-Clark Global and in Canada by Kimberly-Clark Inc.

  • Brand
    Kimberly-Clark
  • Product
    Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Label

    Look for the product code 91590 or UPC 0 36000 91592 1 on the label to confirm if it's the correct product.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide in the US. Product also distributed in Canada.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 8 months after the firm started it.

1. Firm started the recall: Feb 1, 202112. FDA classified it Class II: Apr 2, 202123. Published in FDA’s Enforcement Report: Apr 14, 202134. FDA terminated the recall: Sep 21, 202142021
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

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-0319-2021 (February 1, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0319-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 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