Humanrace recalls SPF 30 sunscreen that doesn't contain the claimed sun protection. Products may not provide adequate UV defense, risking sunburn and skin damage. Check NDC 82779-01 and lots 1732A-D for affected items.
Subpotent Drug: Product does not contain SPF that is declared on the label.
Humanrace is recalling its SPF 30 sunscreen because it doesn't contain the sun protection level it claims. Using this product could lead to inadequate UV protection and increased risk of sunburn or skin damage.
The sunscreen product does not contain the sun protection factor (SPF) it claims on the label. This means it may not provide adequate UV protection, increasing the risk of sunburn and skin damage when exposed to sunlight.
People who own or use Humanrace Suncare SPF 30 sunscreen with NDC 82779-01 and lots 1732A-D through 1742D are affected. Those most at risk are individuals who rely on this product for sun protection.
Check for the product name 'Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30' in a 53mL bottle. Look for NDC 82779-01 and lots 1732A-D through 1742D.
Verify the product's NDC number (82779-01) and lot numbers (1732A-D, 1742A-D) to confirm it is affected.
The product does not contain the SPF it claims, so it may not provide adequate sun protection. Using it could increase the risk of sunburn and skin damage.
Check for the NDC number 82779-01 and lot numbers 1732A-D or 1742A-D on the product label.
The recall does not specify a remedy, so you can check with Humanrace for guidance if you have the affected product.
We’ve drafted a message you can send Humanrace to request your refund or repair — edit it as you like.
Subject: Recall D-1175-2023 — Humanrace Humanrace Hello, I own a Humanrace that is covered by recall D-1175-2023 from Humanrace. 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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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.
