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Class III: unlikely to cause harmTerminated

Advantice Health Dermoplast Anesthetic PAIN & ITCH Recall

Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0

Advantice Health · Cedar Knolls, NJ

Risk level
Class III
Reported by FDA
May 8, 2019
Recall ID
D-1280-2019
Check your lot numberHow we source this data

Summary

Advantice Health recalled Dermoplast Anesthetic PAIN & ITCH starting Apr 25, 2019. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-1280-2019 on May 8, 2019. Reason: Labeling: Not Elsewhere Classified: Full cases may contain canisters that incorrectly state the net weight is 2.75 oz. rather than the correct net weight of 2.0 oz. Status: Terminated.

Why it was recalled

Labeling: Not Elsewhere Classified: Full cases may contain canisters that incorrectly state the net weight is 2.75 oz. rather than the correct net weight of 2.0 oz.

Product description

Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0.5%; full case of 12-2 oz. cans only; Distributed by Moberg Pharma North America LLC, Cedar Knolls, NJ 07927; Product Code 80-6802; Case UPC 1 03 16864 68002 7.

Lot numbers, UPCs & expiration codes

Lot #: 14049A, Exp 12/21

Where it was sold

Nationwide in the USA

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-1280-2019
Classification
Class III
Status
Terminated
Recall initiated
Apr 25, 2019
FDA report date
May 8, 2019
Quantity
111,492 canisters total
Recall type
Voluntary: Firm initiated
Recalling firm
Advantice Health

Original FDA data

Every field from FDA enforcement report D-1280-2019, exactly as published.

Show all FDA fields
City
Cedar Knolls
State
NJ
Status
Terminated
Country
United States
Event ID
82709
Address
7 E Frederick Pl Ste 100
Code information
Lot #: 14049A, Exp 12/21
Postal code
07927-1815
Report date
May 8, 2019
Product type
Drugs
Recall number
D-1280-2019
Classification
Class III
Recalling firm
Advantice Health
Product quantity
111,492 canisters total
Termination date
Feb 11, 2021
Reason for recall
Labeling: Not Elsewhere Classified: Full cases may contain canisters that incorrectly state the net weight is 2.75 oz. rather than the correct net weight of 2.0 oz.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters, 20%, 0.5%; full case of 12-2 oz. cans only; Distributed by Moberg Pharma North America LLC, Cedar Knolls, NJ 07927; Product Code 80-6802; Case UPC 1 03 16864 68002 7.
Distribution pattern
Nationwide in the USA
Recall initiation date
Apr 25, 2019
Initial firm notification
Letter
Center classification date
May 14, 2019

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1280-2019, published May 8, 2019. View the source record (openFDA) · FDA enforcement reports

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

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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