PlainRecalls
FDA Drug Low Class III Terminated

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.

Reported: May 8, 2019 Initiated: April 25, 2019 #D-1280-2019

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.

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.

Details

Recalling Firm
Advantice Health
Units Affected
111,492 canisters total
Distribution
Nationwide in the USA
Location
Cedar Knolls, NJ

Frequently Asked Questions

What product was recalled?
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.. Recalled by Advantice Health. Units affected: 111,492 canisters total.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Drug on May 8, 2019. Severity: Low. Recall number: D-1280-2019.