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RECALL RECORD — CLASS IIIRecall closedD-151-2013/FDA enforcement
Estee Lauder INC·Cosmetics·Oct 23, 2012

Estee Lauder Daywear Sheer Tint Release, Advanced Multi-protection Anti-oxidant Moisturizer…

What you need to know

Class III

  • What happened

    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.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. The product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

  • Action required

    Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement.

Recall closed · classified by the FDANationwide (US)More cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameEstee Lauder INC
Recalling firmEstee Lauder INCNew York, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • A70, A80, AA0, B11, A31, A51, B51, A81, A91, A12, A22, A72, BA0, AB0, BB0, CB0, AC0, BC0, A11, A21, B21, B31, A41.
Distribution area
Nationwide

Nationwide, Puerto Rico, Bermuda and Panama

United States, Puerto Rico

Quantity affected1.7 oz. 241, 236 tubes; 1.5 mL sample size 544, 548 foil packs
Recall initiationFDA report date: February 13, 2013
FDA recall numberD-151-2013

Beyond the headline

The recall, in context

Estee Lauder INC initiated this cosmetics recall on October 23, 2012. The FDA enforcement report states: 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. The FDA report lists distribution as: Nationwide, Puerto Rico, Bermuda and Panama.

The FDA enforcement report describes the reason as: 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.

Estee Lauder Daywear Sheer Tint Release, Advanced Multi-protection Anti-oxidant Moisturizer… was made or distributed by Estee Lauder INC in New York, NY, United States. This page reflects FDA report D-151-2013, dated February 13, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, the product may not deliver the sun protection stated on its label, increasing the risk of sunburn and UV exposure.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

What to do now

  1. 1

    Stop using it

    Set the product aside and do not apply it.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Estee Lauder Daywear Sheer Tint Release, Advanced Multi-protection Anti-oxidant Moisturizer… recall?

Estee Lauder INC recalled Estee Lauder Daywear Sheer Tint Release, Advanced Multi-protection Anti-oxidant Moisturizer… in an FDA Class III enforcement action reported as D-151-2013. 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.

What should I do if I bought this product?

Stop applying or using the product. Check the UPC and lot codes below, then return it to the retailer or contact the manufacturer about a refund or replacement. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Estee Lauder INC recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-151-2013. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.