CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 — Class III drug recall D-1477-2016
Terminated recall by Clinique International, reported 2016-09-07, distributed nationwide. Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specificatio
| Recall number | D-1477-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Clinique International, New York, NY, United States |
| Recall initiated | 2016-05-17 |
| Classified | 2016-08-26 |
| Reported by FDA | 2016-09-07 |
| Terminated | 2018-06-14 |
| Distributed | Nationwide (US) |
| Quantity | 1,771,244 bottles |
| Reason classes | potency |
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
Reason for recall
Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and octisalate, are below the specifications for assay.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1477-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.