Bull Frog SPF 50 Sunscreen Recalled for Out-of-Specification Active Ingredient
ARG Laboratories is recalling Bull Frog SPF 50 Amphibious Lotion nationwide due to the active ingredient being out of specification. Consumers with affected lots should not use the product and contact the manufacturer.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II recall involving an active ingredient out of specification. No illnesses or injuries have been reported. This represents a quality control defect requiring corrective action, with potential but unconfirmed risk to consumers.
Plain-English summary
Bull Frog SPF 50 Amphibious Lotion with Water Armor Tech is being recalled because the active ingredient is out of specification. The affected product was manufactured by ARG Laboratories, Inc. and distributed nationwide by Bullfrog Brands LLC. A total of 9,697 units have been identified as affected.
The recalled product is the 5 FL OZ (148ML) bottle with UPC 8 50016 52112 5. The affected lot codes are 08623C2 and 08923C2, with an expiration date of 03/31/2026.
Consumers who have purchased Bull Frog SPF 50 Amphibious Lotion with the affected lot codes should stop using the product immediately. Contact ARG Laboratories, Inc. or Bullfrog Brands LLC for instructions on returning the product or obtaining a refund. If you have questions, consult with a healthcare provider or pharmacist.
The recalled product
- Product
- Bull Frog SPF 50 Amphibious Lotion SPF 50 Amphibious Lotion with Water Armor Tech, Broad Spectrum Sunscreen with UVA/UVB Protection, NEW WT. 5 FL OZ (148ML), Distributed by: Bullfrog Brands LLC, PO Box 600207, Dallas, TX 75360 USA. UPC 8 50016 52112 5
- Manufacturer
- ARG Laboratories, Inc.
- Category
- Drug — Sunscreen
- Hazard
- Affected units
- 9,697
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Lot 08623C2
- 08923C2
- Exp 03/31/2026
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 11 recalled by ARG Laboratories, Inc. under a single FDA (Drugs) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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