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Class III: unlikely to cause harmTerminated

Johnson & Johnson Clean & Clear advantage Recall

Clean & Clear advantage, 3-in-1 foaming wash 8 FL

Johnson & Johnson · Skillman, NJ

Risk level
Class III
Reported by FDA
Dec 26, 2012
Recall ID
D-098-2013
Check your lot numberHow we source this data

Summary

Johnson & Johnson recalled Clean & Clear advantage starting Dec 4, 2012. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-098-2013 on Dec 26, 2012. Reason: Superpotent (Single Ingredient Drug): salicylic acid. Status: Terminated.

Why it was recalled

Superpotent (Single Ingredient Drug): salicylic acid

Product description

Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the US by: Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. Skillman, NJ 08558-9418 NDC 58232-0326-8

Lot numbers, UPCs & expiration codes

0142VA, 0132VB, 0112VC, 0122VB, 0102VA, 0102VB, 0112VB 0122VA, 0092VB, 0112VA, 0092VA, 0082VA, 0072VA, 0062VA 0062VB, 0052VA, 0052VB, 0042VA, 0032VA, 0022VA, 0012VA, 0171VA, 0171VB, 0161VB, 0151VA, 0161VA, 0141VA, 0131VA 0131VB, 0121VA, 0111VA, 0101VA, 0091VA, 0081VB, 0081VA 0071VA, 0061VA, 0051VB, 0051VA, 0041VA, 0031VA, 0021VB 0011VC, 0011VB, 0190VA, 0011VA, 0180VB, 0170VB, 0180VA 0722RT, 0732RT, 0742RT, 0752RT, 1722RD, 1732RD, 1772RD 1782RD, 1792RD, 1802RD, 1802RDA, 1812RD, 1822RD, 0092RD, 0102RD, 0112RD, 0122RD, 0132RD, 0142RD, 0162RD 0172RD, 0182RD, 0192RD, 0212RD, 0202RD, 0062RD, 1451RD 1461RD, 1461RDA, 1511RD, 1521RD, 1531RD, 1661RD, 1481RD, 1571RD, 1581RD, 1591RD, 1601RD, 1611RD, 1621RD 1681RD, 1532RD, 1522RD, 1842RD, 1512RD, 1522RD, 1562RD 1582RD, 1572RD, 1722RD, 1732RD, 1742RD, 1772RD, 1782RD 1792RD, 1802RD, 1812RD, 1812RDA, 1822RD, 1842RD, 1852RD, 1872RD

Where it was sold

Nationwide

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-098-2013
Classification
Class III
Status
Terminated
Recall initiated
Dec 4, 2012
FDA report date
Dec 26, 2012
Quantity
1,474,462 bottles
Recall type
Voluntary: Firm initiated
Recalling firm
Johnson & Johnson

Original FDA data

Every field from FDA enforcement report D-098-2013, exactly as published.

Show all FDA fields
City
Skillman
State
NJ
Status
Terminated
Country
United States
Event ID
63787
Address
199 Grandview Rd
Code information
0142VA, 0132VB, 0112VC, 0122VB, 0102VA, 0102VB, 0112VB 0122VA, 0092VB, 0112VA, 0092VA, 0082VA, 0072VA, 0062VA 0062VB, 0052VA, 0052VB, 0042VA, 0032VA, 0022VA, 0012VA, 0171VA, 0171VB, 0161VB, 0151VA, 0161VA, 0141VA, 0131VA 0131VB, 0121VA, 0111VA, 0101VA, 0091VA, 0081VB, 0081VA 0071VA, 0061VA, 0051VB, 0051VA, 0041VA, 0031VA, 0021VB 0011VC, 0011VB, 0190VA, 0011VA, 0180VB, 0170VB, 0180VA 0722RT, 0732RT, 0742RT, 0752RT, 1722RD, 1732RD, 1772RD 1782RD, 1792RD, 1802RD, 1802RDA, 1812RD, 1822RD, 0092RD, 0102RD, 0112RD, 0122RD, 0132RD, 0142RD, 0162RD 0172RD, 0182RD, 0192RD, 0212RD, 0202RD, 0062RD, 1451RD 1461RD, 1461RDA, 1511RD, 1521RD, 1531RD, 1661RD, 1481RD, 1571RD, 1581RD, 1591RD, 1601RD, 1611RD, 1621RD 1681RD, 1532RD, 1522RD, 1842RD, 1512RD, 1522RD, 1562RD 1582RD, 1572RD, 1722RD, 1732RD, 1742RD, 1772RD, 1782RD 1792RD, 1802RD, 1812RD, 1812RDA, 1822RD, 1842RD, 1852RD, 1872RD
Postal code
08558-1311
Report date
Dec 26, 2012
Product type
Drugs
Recall number
D-098-2013
Classification
Class III
Recalling firm
Johnson & Johnson
Product quantity
1,474,462 bottles
Termination date
Apr 29, 2014
Reason for recall
Superpotent (Single Ingredient Drug): salicylic acid
Voluntary / mandated
Voluntary: Firm initiated
Product description
Clean & Clear advantage, 3-in-1 foaming wash 8 FL. OZ. (240 mL) bottle, OTC, Distributed in the US by: Johnson & Johnson Consumer Products Company Division of Johnson & Johnson Consumer Companies Inc. Skillman, NJ 08558-9418 NDC 58232-0326-8
Distribution pattern
Nationwide
Recall initiation date
Dec 4, 2012
Initial firm notification
Letter
Center classification date
Dec 20, 2012

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-098-2013, published Dec 26, 2012. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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