LA FRESH travel lite Sunnyside Lotion Wipe silky — Class II drug recall D-1566-2019
Terminated recall by La Fresh Group, Inc., reported 2019-07-31. Marketed without an Approved NDA/ANDA: The product may be construed a sunscreen due to labeling of the product
| Recall number | D-1566-2019 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | La Fresh Group, Inc., Chino, CA, United States |
| Recall initiated | 2019-07-15 |
| Classified | 2019-07-31 |
| Reported by FDA | 2019-07-31 |
| Terminated | 2021-04-09 |
| Quantity | 83,050 packets |
| Reason classes | labeling, unapproved product |
Product
LA FRESH travel lite Sunnyside Lotion Wipe silky, non-greasy formula smooth, soft & moisturizing featuring titanium dioxide, 1 wipe individually wrapped packet, 4.75" x 5.75" (12.0 cm x 14.6 cm) Ingredients: Water, Dimethicone, Dimethiconol, Titanium Dioxide, Benzophenone-3, Octinoxate, Ethylhexylglycerine, Phenoxyethanol, Distributed by La Fresh Group, Inc. Chino, CA 91710 www.LaFreshGroup.com
Reason for recall
Marketed without an Approved NDA/ANDA: The product may be construed a sunscreen due to labeling of the product and comments about the product found on e-commerce websites.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1566-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.