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ACTIVE RECALL — CLASS IIIActive recallD-0237-2017/FDA enforcement
Cipher Pharmaceuticals US LLC·Cosmetics·Dec 6, 2016

Inova (Benzoyl Peroxide) 4%, Easy Pad (Tocopherol) 5%, for Topical Use Only, Packaged in a Box…

What you need to know

Class III

  • What happened

    Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • 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.

Active recall · classified by the FDAAZ, CO, OHMore cosmetics

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Match before you discard

Product identification

Source: FDA COSMETICS

Brand nameCipher Pharmaceuticals US LLC
Recalling firmCipher Pharmaceuticals US LLCDaniel Island, SC, United States
UPC / barcodes
0 26871 20130 1
Lot / date codes
  • Lot #01316L02 6871201301
Distribution area
AZCOOH

AZ, CO and OH.

United States

Quantity affected216 boxes
Recall initiationFDA report date: January 4, 2017
FDA recall numberD-0237-2017

Beyond the headline

The recall, in context

Cipher Pharmaceuticals US LLC initiated this cosmetics recall on December 6, 2016. The FDA enforcement report states: Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications. The FDA report lists distribution as: AZ, CO and OH.

The FDA enforcement report describes the reason as: Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications.

Inova (Benzoyl Peroxide) 4%, Easy Pad (Tocopherol) 5%, for Topical Use Only, Packaged in a Box… was made or distributed by Cipher Pharmaceuticals US LLC in Daniel Island, SC, United States. This page reflects FDA report D-0237-2017, dated January 4, 2017.

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, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

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 UPC and lot code 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 Inova (Benzoyl Peroxide) 4%, Easy Pad (Tocopherol) 5%, for Topical Use Only, Packaged in a Box… recall?

Cipher Pharmaceuticals US LLC recalled Inova (Benzoyl Peroxide) 4%, Easy Pad (Tocopherol) 5%, for Topical Use Only, Packaged in a Box… in an FDA Class III enforcement action reported as D-0237-2017. Subpotent Drug: Product label claim is 4% Benzoyl Peroxide, Initial Stability testing showed variation within the lot outside of product specifications.

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 Cipher Pharmaceuticals US LLC?

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-0237-2017 and keep the packaging, lot code and proof of purchase if you have them.

Is the Cipher Pharmaceuticals US LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record D-0237-2017. 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.