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Lower risk Drug recall · FDA · Published July 15, 2019

La Fresh Sunnyside Lotion Wipe: Sunscreen Mislabeling Risk

La Fresh recalls Sunnyside Lotion Wipe due to potential sunscreen mislabeling without FDA approval. Check product lot numbers starting with 453091 for affected items.

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

🇺🇸 FDA recall #D-1566-2019DrugLa Fresh ›
Take action

Contact the company

Official pagewww.LaFreshGroup.comAlso onlinewww.Amazon.com
Recalling firmLa Fresh Group, Inc.4651 Schaefer Ave · Chino, CA 91710-5542
✎ GovInfoNow plain-language explainer

La Fresh is recalling Sunnyside Lotion Wipe because it may be mislabeled as a sunscreen without proper FDA approval. This could lead to users not getting the intended product benefits or missing sun protection. Read more at govinfonow.com/recall/38280-la-fresh-sunnyside-lotion-wipe-sunscreen-mislabeling-risk.

Source Summary by GovInfoNow · govinfonow.com/recall/38280-la-fresh-sunnyside-lotion-wipe-sunscreen-mislabeling-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-1566-2019

Cite this page

“La Fresh Sunnyside Lotion Wipe: Sunscreen Mislabeling Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/38280-la-fresh-sunnyside-lotion-wipe-sunscreen-mislabeling-risk. Based on FDA recall #D-1566-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1566-2019%22&limit=1).

The Food and Drug Administration announced on July 15, 2019, that La Fresh Group, Inc. recalled LA FRESH travel lite Sunnyside Lotion Wipes because they were marketed without an approved New Drug Application or Abbreviated New Drug Application. The agency stated the product may be construed as a sunscreen due to its labeling and online comments.

How to tell if you have it

  • Brand: La Fresh
  • Product name: LA FRESH travel lite Sunnyside Lotion Wipe silky, non-greasy formula smooth, soft & moisturizing featuring titanium dioxide
  • Lot codes: All lots beginning with 453091
  • Distribution: Firm's website sales and www.Amazon.com

The hazard

The FDA said the product was marketed without an Approved NDA/ANDA. The agency noted that the labeling of the product and comments about it found on e-commerce websites may cause it to be construed as a sunscreen.

Context

GovInfoNow's records show other recent recalls of similar products include Allies Group Recalls SPF 50 Invisible Sunscreen Gel Due to Subpotent Protection (2026-08-14), MENOW SPF35 Sunscreen Powder Recall: CPG Deviations (2026-08-08), and Allies Group Recalls Invisible Sunscreen Gel Due to SPF 50 Protection Risk (2026-08-14).

How to tell if you have this one

Check the product label for lot numbers starting with 453091. The item is a travel-sized lotion wipe with titanium dioxide and sold by La Fresh Group, Inc.

  • Brand
    La Fresh
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers starting with 453091 on the product label.

How this recall unfolded

Recall timeline

FDA terminated this recall 21 months after the firm started it.

1. Firm started the recall: Jul 15, 201912. FDA classified it Class II: Jul 31, 201923. Published in FDA’s Enforcement Report: Jul 31, 201934. FDA terminated the recall: Apr 9, 2021420192021
  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.

Take action

Contact La Fresh

We’ve drafted a message you can send La Fresh to request your refund or repair — edit it as you like.

✉️ Open in emailCompany site
Subject: Recall D-1566-2019 — La Fresh Sunnyside Lotion Wipe: Sunscreen Mislabeling Risk

Hello,

I own a La Fresh Sunnyside Lotion Wipe: Sunscreen Mislabeling Risk that is covered by recall D-1566-2019 from La Fresh.

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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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-1566-2019 (July 15, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1566-2019 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.
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