RecallRadar

FDA Drug recall D-1175-2023

Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% m…

On 2023-09-27 the FDA classified a Class II recall of Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% m… by Humanrace, citing subpotent Drug: Product does not contain SPF that is declared on the label.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1175-2023
ClassificationClass II
Statusongoing
Initiated2023-08-18
Published2023-09-27
Last updated2026-09-13 11:52 UTC
CompanyHumanrace
DistributionUS

Product

Humanrace Suncare, Ozone Face Protection Daily Moisturizer, Broad Spectrum Sunscreen SPF 30, packaged as a 53mL (1.8 fl oz.) bottle, 100% mineral, Active Ingredient: Zinc oxide 15%, Snow Mushroom, Dist. By: @Humanrace 2022 Beverly Hills, CA 90210, USA, NDC 82779-01

Reason

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

Identifiers

code_infoLot #: 1732A, 1732B, 1742A, 1742B, 1742C, 1742D; Exp. 06/2024.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1175-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.