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Use caution Drug recall · FDA · Published May 17, 2016

Clinique Moisture Surge Recall: Subpotent Sunscreen Ingredients

Clinique recalls Moisture Surge Tinted Moisturizer SPF 15 because active sunscreen ingredients are below specification. Check your UPC and shade.

🇺🇸 FDA recall #D-1476-2016DrugClinique ›
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Recalling firmClinique International767 5th Ave · New York, NY 10153-0023
✎ GovInfoNow plain-language explainer

What happened, in plain English

Clinique International has recalled the Moisture Surge Tinted Moisturizer Broad Spectrum SPF 15 because two active sunscreen ingredients, octinoxate and octisalate, are subpotent. This means the product may not provide the level of sun protection indicated on the label. The recall affects all lots of this specific 1 FL. OZ./30 ml bottle. Read more at govinfonow.com/recall/42624-clinique-moisture-surge-recall-subpotent-sunscreen-ingredients.

Source Summary by GovInfoNow · govinfonow.com/recall/42624-clinique-moisture-surge-recall-subpotent-sunscreen-ingredients · Updated October 9, 2026 · FDA enforcement record: FDA #D-1476-2016

Cite this page

“Clinique Moisture Surge Recall: Subpotent Sunscreen Ingredients.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/42624-clinique-moisture-surge-recall-subpotent-sunscreen-ingredients. Based on FDA recall #D-1476-2016 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1476-2016%22&limit=1).

Why it’s dangerous

The active sunscreen ingredients octinoxate and octisalate are below the required assay specifications. This subpotency means the product might not protect your skin from UV rays as effectively as claimed, potentially leading to sunburn or long-term sun damage during normal use.

Who’s affected

Consumers who purchased Clinique Moisture Surge Tinted Moisturizer Broad Spectrum SPF 15 in the 1 FL. OZ./30 ml bottle size, specifically Shade 04 (M-N) and other shades distributed nationwide.

How to tell if you have this one

Look for a Clinique Moisture Surge Tinted Moisturizer Broad Spectrum SPF 15 bottle containing 1 FL. OZ.LIQ./30 ml. Check the UPC No. 20714-47479-9 and verify if your shade matches Shade 04 (M-N) or other shades included in the recall of all lots.

  • Brand
    Clinique
  • Product
    CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique
  • Category
    Drug
FDA recall event · 6 products

All 6 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class III
  • Status
    Terminated
  • Distribution
    Nationwide
Recall numberProduct, codes & lots
D-1473-2016CLINIQUE 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. 20714-47476-8, Shade 01 (VF-N); all lots
D-1474-2016CLINIQUE 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. 20714-47477-5, Shade 02 (VF-N); all lots
D-1475-2016CLINIQUE 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. 20714-47478-2, Shade 03 (MF-N); all lots
D-1476-2016CLINIQUE 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. 20714-47479-9, Shade 04 (M-N); all lots
D-1477-2016CLINIQUE 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); all lots
D-1478-2016CLINIQUE 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. 20714-48241-1, Shade 06 (D-G); all lots
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product

    Verify that you have the Clinique Moisture Surge Tinted Moisturizer Broad Spectrum SPF 15 in a 1 FL. OZ./30 ml bottle with UPC No. 20714-47479-9.

  2. Discontinue Use

    Stop using the product immediately as the sunscreen ingredients are subpotent and may not provide adequate protection.

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.1 years after the firm started it.

1. Firm started the recall: May 17, 201612. FDA classified it Class III: Aug 26, 201623. Published in FDA’s Enforcement Report: Sep 7, 201634. FDA terminated the recall: Jun 14, 2018420162018
  1. Firm started the recall
  2. FDA classified it Class III
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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.

  • Official source: FDA Recall #D-1476-2016 (May 17, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1476-2016 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA