CLASS II Drug recall · Reported 25 Jul 2018 · FDA Enforcement Report

alba Botanica sport mineral sunscreen recalled

The Hain Celestial Group Inc. - Worldwide HQ is recalling alba Botanica sport mineral sunscreen (titanium dioxide 7.0% and zinc oxide 9.0%), spf 45, distributed nationwide in the US. The recall was initiated on 5 Jul 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Codes: a) 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A; and b) 7353
Quantity recalled47,128 tubes

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0920-2018
FDA event ID
80473
Recalling firm
The Hain Celestial Group Inc. - Worldwide HQ, New Hyde Park, NY
Classification
Class II
Status
Terminated
Recall initiated
5 Jul 2018
FDA classified
13 Jul 2018
Reported
25 Jul 2018
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Packaging Defects

Timeline

5 Jul 2018Recall initiated by company
13 Jul 2018Classified by FDA+8 days
25 Jul 2018Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Incorrect Product Formulation: wrong sunscreen product in the package.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

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.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

Incorrect Product Formulation: wrong sunscreen product in the package.

Which lots are affected?

Lot Codes: a) 7363B, 7363I, 8002C, 8002I, 8054J, 8055B, 8174A; and b) 7353

Where was it sold?

Nationwide in the USA

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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