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ACTIVE RECALL — CLASS IIActive recallD-1176-2023/FDA enforcement
Humanrace·Cosmetics·Aug 18, 2023

Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, Packaged as a 148ml (5…

What you need to know

Class II

  • What happened

    Subpotent Drug: Product does not contain SPF that is declared on the label.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. The product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Active recall · classified by the FDANationwide (US)More cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameHumanrace
Recalling firmHumanraceBeverly Hills, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #: 1752A, 1752B, 1782E, 1782G, 1782C, 1752C, 1782B
  • Exp. 06/2024.
Distribution area
Nationwide

Nationwide in the USA, Spain, Italy, UK, and France.

United States, United Kingdom, France

Quantity affected2942 units
Recall initiationFDA report date: September 27, 2023
FDA recall numberD-1176-2023

Beyond the headline

The recall, in context

Humanrace initiated this cosmetics recall on August 18, 2023. The FDA enforcement report states: Subpotent Drug: Product does not contain SPF that is declared on the label. The FDA report lists distribution as: Nationwide in the USA, Spain, Italy, UK, and France.

The FDA enforcement report describes the reason as: Subpotent Drug: Product does not contain SPF that is declared on the label.

Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, Packaged as a 148ml (5… was made or distributed by Humanrace in Beverly Hills, CA, United States. This page reflects FDA report D-1176-2023, dated September 27, 2023.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, the product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, Packaged as a 148ml (5… recall?

Humanrace recalled Suncare, Ozone Body Protection Cream, Broad Spectrum Sunscreen SPF 30, Packaged as a 148ml (5… in an FDA Class II enforcement action reported as D-1176-2023. Subpotent Drug: Product does not contain SPF that is declared on the label.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Humanrace recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-1176-2023. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Humanrace

View brand
Class II·

Humanrace

Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, Packaged As…

Subpotent Drug: Product does not contain SPF that is declared on the label.

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.