Hain Celestial Recalls alba BOTANICA Sunscreen Due to Incorrect Formulation
The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen because the wrong product formulation was placed in the packages.
The agency’s classification
FDA (Drugs): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the hazard involves a formulation error without reported injuries or illnesses, fitting the criteria for a moderate severity score.
Plain-English summary
The Hain Celestial Group, Inc. is recalling 47,128 tubes of alba BOTANICA sport mineral sunscreen (SPF 45). The product is packaged in 4-tube cases or 8-pack shipper displays and was distributed nationwide in the USA.
The recall was initiated due to an incorrect product formulation, specifically because the wrong sunscreen product was placed in the packages. The affected lot codes are 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A, and 7353.
Consumers should check their inventory for these specific lot codes and stop using the product if it matches the recalled description.
The recalled product
- Product
- alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged in a) 4 tubes per case; b) 8 pack shipper display; Manufactured By: The Hain Celestial Group, Inc., Lake Success, NY 11042, UPC 7 24742 01102 4.
- Manufacturer
- The Hain Celestial Group, Inc. - Worldwide HQ
- Category
- Drug — Sunscreen
- Affected units
- 47,128
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 (8)
- Lot Codes: a) 7363B
- 7363I
- 8002C
- 8002I
- 8054J
- 8055B
- 8174A
- and b) 7353
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · The Hain Celestial Group, Inc. - Worldwide HQ
See all →- Severealba BOTANICA Sunscreen Recalled for Microbial Contamination
FDA (Drugs) · 2018-08-22
- LowHain Celestial Recalls BluePrint Organic Beet Blast Drinks Due to Labeling Error
FDA (Food) · 2017-12-27
- SevereMaraNatha Sunflower Seed Butter Recalled for Listeria Contamination Risk
FDA (Food) · 2016-08-03
Same hazard · mis labeling
See all →- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-10-14
- SevereBetter Bakehouse Recalls Donutful Chocolate Dipped Vanilla Cake Donuts for Undeclared Milk
FDA (Food) · 2026-10-14
- HighFreshPoint Recalls Cranberry Chicken Salad Wedges for Undeclared Egg Allergen
FDA (Food) · 2026-10-14
- HighJ K Patisserie & Bakery LLC Recalls Croissants for Undeclared Egg
FDA (Food) · 2026-10-14
- ModerateHalyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
FDA (Devices) · 2026-10-14
Similar recalls
- Severealba BOTANICA Sunscreen Recalled for Microbial Contamination
FDA (Drugs) · 2018-08-22
- LowHain Celestial Recalls BluePrint Organic Beet Blast Drinks Due to Labeling Error
FDA (Food) · 2017-12-27
- ModerateMineral sunscreen recalled over current good manufacturing practice deviations
FDA (Drugs) · 2025-12-03
- ModerateSchwab mineral sunscreen recalled over manufacturing practice deviations at Botana
FDA (Drugs) · 2025-12-03
- ModerateGabriel mineral sunscreen recalled over manufacturing practice deviations
FDA (Drugs) · 2025-12-03
- HighKids by babyganics mineral sunscreen recalled for chemical contamination
FDA (Drugs) · 2025-03-19