FDA recall, , Moderate risk
The One SPF 50 Invisible Sunscreen Gel
THE ONE SPF 50 INVISIBLE SUNSCREEN GEL may not reliably provide the SPF 50 protection stated on the label.
Summary by Recall Canary from the FDA notice
What happened
Allies Group Inc. of Wilmington, Delaware, recalled The One SPF 50 Invisible Sunscreen Gel because firm testing indicated the affected product may not reliably provide the SPF 50 protection stated on the label. The recall began August 14, 2026, and was added to the FDA's Enforcement Report on August 28, 2026.
The product was distributed nationwide within the U.S.A. The recalled items include 90ml, 20ml, 50ml tubes and 3ml sachets, all labeled as made in the U.S.A. and distributed by Allies Group Pte Ltd, Singapore 068914.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medicine recalls:
- Check the FDA or company notice for instructions specific to this product.
- Ask your pharmacist or doctor whether your lot is affected and what to do.
Is your tube affected?
4 products
Match the lot code and UPC listed under your product.
A UPC is the number printed under a barcode.
The One SPF 50 Invisible Sunscreen Gel, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 90ml - 3 fl. oz. Tube
- UPC
- 8 885014 075853
- Lot code
- G23W03B
The One SPF 50 Invisible Sunscreen Gel, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 20ml - 0.7 fl. oz. Tube
- UPC
- 8 885014 074733
- Lot code
- H22V02A
The One SPF 50 Invisible Sunscreen Gel, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 50ML - 1.7 fl. oz Tube
- UPC
- 8 885014 073224
- Lot code
- H22V01
- H22V02
- K22V02A
- M10V01
- G23W02B
- G23W03
- G23W03D
- K10W01A
- K10W01C
- M11W02
- F09X02
The One SPF 50 Invisible Sunscreen Gel, (Avobenzone 3%, Homosalate 7%, Octocrylene 10%, Octisalate 5%), 3ml - 0.1 fl. oz, Sachet: Single use only
- UPC
- 8 885014 073293
- Lot code
- C13W01A
Recall details
- Company began the recall
- Sold in
Nationwide within the U.S.A
- Company
- Allies Group Inc.Wilmington, Delaware
- Hazard
- Wrong drug strength
- Risk
Moderate risk
Taking it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99652
- Recall numbers
- D-0823-2026 to D-0826-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report
Listed on Recall Canary
Classified by FDA
In FDA's weekly enforcement report
Summary updated
