# FDA recall D-151-2013

> **Estee Lauder Inc** · Class III · drug recall initiated 2012-10-23.

## Product

ESTEE LAUDER DayWear Sheer Tint Release, Advanced Multi-Protection Anti-Oxidant  Moisturizer Broad Spectrum SPF15, All Skin types, 1.7 FL. OZ. LIQ/50 ml (tube inside a unit carton) with UPC No. 2713179904, Code WKEM-01, and 1.5 mL foil sample packets,  ESTEE LAUDER, DIST., NEW YORK, N.Y. 10022 NDC 11559-008-01

## Reason for recall

Failed Stability Specifications: The active sunscreen ingredient, avobenzone 3%, may not be stable over the shelf life, the sunscreen effectiveness may be less than labeled.

## Distribution

Nationwide, Puerto Rico, Bermuda and Panama

## Key facts

- **Recall number:** D-151-2013
- **Recalling firm:** Estee Lauder Inc
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2012-10-23
- **Report date:** 2013-02-13
- **Termination date:** 2017-04-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** New York, NY, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-151-2013

## Citation

> AI Analytics. FDA recall D-151-2013. Retrieved 2026-05-25 from https://api.ai-analytics.org/recall/D-151-2013. Source: US FDA. Licensed CC0.

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