Unrated Drug recall · FDA · Published August 14, 2020

SkinGuard 24 Hand Sanitizer Recall: Unapproved Methanol Content

SG24 LLC recalls SkinGuard 24 All-Day Hand Sanitizer bottles containing unapproved methanol. The product was marketed without FDA approval and contains 0.56% methanol, making it an unapproved new drug.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #D-1572-2020Drug SG24 LLC ›

Recall notice

Marketed without an Approved NDA/ANDA; product labeled to contain 0.56% methanol making it an unapproved new drug

Take action

Contact the company

Recalling firmSG24 LLC8315 Rivoli Road, Ste A · Bolingbroke, GA 31004

✎ GovInfoNow plain-language explainer

SG24 LLC is recalling SkinGuard 24 All-Day Hand Sanitizer bottles that contain unapproved methanol. This product was marketed without FDA approval and is considered an unapproved new drug due to its methanol content. Read more at govinfonow.com/recall/36836-skinguard-24-hand-sanitizer-recall-unapproved-methanol-content.

Source Summary by GovInfoNow · govinfonow.com/recall/36836-skinguard-24-hand-sanitizer-recall-unapproved-methanol-content · Updated October 5, 2026 · FDA enforcement record: FDA #D-1572-2020

Cite this page

“SkinGuard 24 Hand Sanitizer Recall: Unapproved Methanol Content.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36836-skinguard-24-hand-sanitizer-recall-unapproved-methanol-content. Based on FDA recall #D-1572-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1572-2020%22&limit=1).

SG24 LLC voluntarily recalled its SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottles on Aug. 14, 2020, after the FDA announced the product was marketed without an approved New Drug Application and contained methanol. The Food and Drug Administration issued the recall under classification D-1572-2020.

How to tell if you have it

Brand: SG24 LLC
Product: SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump
UPC: 793573147125
SKU: 051230024
Lots: All lots labeled to contain methanol
Quantity: 9600 bottles
Distribution: Nationwide

The hazard

The FDA stated the product was marketed without an approved New Drug Application or Abbreviated New Drug Application. The label indicated the sanitizer contained 0.56% methanol, classifying it as an unapproved new drug.

Context

GovInfoNow's records show other recent recalls of similar products include SUN PHARMACEUTICAL Xyvona 3mg Tablets Recall: FDA Denial of Marketing (2026-05-22), Haleon Gas-X Extra Strength Softgels Recall: Chemical Contamination Risk (2026-06-04), and Zep Alcohol Sanitizer Spray Recall: Microbial Contamination Risk (2026-05-22).

How to tell if you have this one

Check for the UPC 793573147125 on the bottle. The product is sold by SG24 LLC in Bolingbroke, GA and contains methanol in all lots.

Brand
SG24 LLC
Category
Drug

FDA recall event · 4 products

All 4 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

Classification
Class I
Status
Terminated
Distribution
Nationwide

Recall number	Product, codes & lots	Quantity
D-1571-2020	SkinGuard 24 All-Day Hand Sanitizer 2.67 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147103; SKU 051220024 All lots labeled to contain methanol	9600 bottles
D-1572-2020	SkinGuard 24 All-Day Hand Sanitizer 8 oz. bottle with foam pump, Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147125; SKU 051230024 All lots labeled to contain methanol	9600 bottles
D-1573-2020	Skin Guard 24 All-Day Hand Sanitizer 10 mL Pocket Pen Dist by: SG24 LLC, Bolingbroke, GA 31004 UPC 793573147097; SKU 051210048 All lots labeled to contain methanol	10,000 pens
D-1574-2020	Skin Guard 24 All-Day Hand Sanitizer 1 4"x6" Hand Sanitizing Towelette packaged in 2.5 x 3.75 packets, Dist by: SG24 LLC, Bolingbroke, GA 31004; SKU 03150025 All lots labeled to contain methanol	122,500 individual wipe packets

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for the UPC 793573147125 on the bottle to confirm it is recalled.

Where it went and when

Where it was distributed

Distributed nationwide.

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.8 years after the firm started it.

Aug 14, 2020Firm started the recall
Sep 9, 2020Published in FDA’s Enforcement Report
Sep 11, 2020FDA classified it Class I
Jun 5, 2023FDA terminated the recall

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

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Link to this recall

<a href="https://govinfonow.com/recall/36836-skinguard-24-hand-sanitizer-recall-unapproved-methanol-content">SkinGuard 24 Hand Sanitizer Recall: Unapproved Methanol Content (GovInfoNow)</a>

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-1572-2020 (August 14, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1572-2020 to see it in context.
Plain-language summary written by qwen3:4b on October 5, 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.