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RECALL RECORD — CLASS IIIRecall closedD-1532-2019/FDA enforcement
Ningbo Huize Commodity Co., LTD.·Cosmetics·Apr 1, 2019

SPF 30 Sunscreen Lotion Active Ingredients Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0%…

What you need to know

Class III

  • What happened

    CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. Current good manufacturing practice failures can affect product identity, strength, quality or purity.

  • 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 FDAINMore cosmetics

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Product identification

Source: FDA COSMETICS

Brand nameNingbo Huize Commodity Co., LTD.
Recalling firmNingbo Huize Commodity Co., LTD.Yuyao, China
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Lot #: 20180709, Exp 07/08/2020
  • 20180710, Exp 07/09/2020
Distribution area
IN

Foreign manufacturer located in China and distributed to seven consignees located in China.

United States, China

Quantity affected10, 000
Recall initiationFDA report date: August 7, 2019
FDA recall numberD-1532-2019

Beyond the headline

The recall, in context

Ningbo Huize Commodity Co., LTD. initiated this cosmetics recall on April 1, 2019. The FDA enforcement report states: CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products. The FDA report lists distribution as: Foreign manufacturer located in China and distributed to seven consignees located in China.

The FDA enforcement report describes the reason as: CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.

SPF 30 Sunscreen Lotion Active Ingredients Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0%… was made or distributed by Ningbo Huize Commodity Co., LTD. in Yuyao, China. This page reflects FDA report D-1532-2019, dated August 7, 2019.

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, current good manufacturing practice failures can affect product identity, strength, quality or purity.

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 SPF 30 Sunscreen Lotion Active Ingredients Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0%… recall?

Ningbo Huize Commodity Co., LTD. recalled SPF 30 Sunscreen Lotion Active Ingredients Octinoxate 7.5%, Octisalate 2.0%, Oxybenzone 4.0%… in an FDA Class III enforcement action reported as D-1532-2019. CGMP deviations: Stability testing was not conducted on manufactured sunscreen and hand sanitizer OTC products.

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Ningbo Huize Commodity Co., LTD.?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall D-1532-2019 and keep the packaging, lot code and proof of purchase if you have them.

Is the Ningbo Huize Commodity Co., LTD. 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-1532-2019. 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

Brand history

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