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Drug recall · FDA · Published July 5, 2018

The Hain Celestial Group, Inc. - Worldwide HQ recalls alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged

The Hain Celestial Group recalls alba BOTANICA sport mineral sunscreen (SPF 45) due to incorrect formulation. This means the wrong sunscreen product was packaged. Consumers should check lot codes and contact the company for details.

🇺🇸 FDA recall #D-0920-2018Drugalba BOTANICA ›
Take action

Contact the company & request your remedy

Recalling firmThe Hain Celestial Group, Inc. - Worldwide HQ1111 Marcus Ave · New Hyde Park, NY 11042-1221
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

The Hain Celestial Group is recalling alba BOTANICA sport mineral sunscreen (SPF 45) because the wrong product was packaged. This could lead to consumers using an incorrect sunscreen formulation, which may not provide the intended protection. Read more at govinfonow.com/recall/40381-alba-botanica-sport-mineral-sunscreen-recall-wrong-product-formulation.

Source Summary by GovInfoNow · govinfonow.com/recall/40381-alba-botanica-sport-mineral-sunscreen-recall-wrong-product-formulation · Updated October 6, 2026 · FDA enforcement record: FDA #D-0920-2018

Cite this page

“alba BOTANICA Sport Mineral Sunscreen Recall: Wrong Product Formulation.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/40381-alba-botanica-sport-mineral-sunscreen-recall-wrong-product-formulation. Based on FDA recall #D-0920-2018 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0920-2018%22&limit=1).

Why it’s dangerous

The recall is for incorrect product formulation, meaning the wrong sunscreen product was packaged. This could result in consumers using a sunscreen that does not meet the intended specifications for protection. The hazard does not involve immediate physical harm but rather potential misuse of an incorrect product.

Who’s affected

Anyone who owns or uses the recalled alba BOTANICA sport mineral sunscreen (SPF 45) tubes. People most at risk are those who have the specific lot codes mentioned in the recall.

How to tell if you have this one

Check the lot codes on the product: a) 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A; and b) 7353. The product is a 170g (6 oz) tube of alba BOTANICA sport mineral sunscreen with SPF 45.

  • Brand
    alba BOTANICA
  • Product
    alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Codes

    Look for lot codes on the product: a) 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A; and b) 7353.

✎ GovInfoNow

Questions people ask

Why is this sunscreen being recalled?

The Hain Celestial Group recalls alba BOTANICA sport mineral sunscreen (SPF 45) due to incorrect product formulation, meaning the wrong sunscreen product was packaged.

What should I do if I have the recalled sunscreen?

Check the lot codes on the product. If it matches the listed lot codes, contact The Hain Celestial Group for further instructions.

Is there a risk of injury from using this sunscreen?

The recall is for incorrect formulation, not a safety hazard that causes injury. The hazard does not involve immediate physical harm.

Take action

Contact alba BOTANICA

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

Subject: Recall D-0920-2018 — alba BOTANICA alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), sp

Hello,

I own a alba BOTANICA sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, 170 g (6 oz) tubes packaged that is covered by recall D-0920-2018 from alba BOTANICA.

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-0920-2018 (July 5, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0920-2018 to see it in context.
  • Plain-language summary written by qwen3:4b on October 6, 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