Dermoplast Anesthetic PAIN & ITCH — Class III drug recall D-1280-2019
Terminated recall by Advantice Health, reported 2019-05-08, distributed nationwide. Labeling: Not Elsewhere Classified: Full cases may contain canisters that incorrectly state the net weight is
| Recall number | D-1280-2019 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Advantice Health, Cedar Knolls, NJ, United States |
| Recall initiated | 2019-04-25 |
| Classified | 2019-05-14 |
| Reported by FDA | 2019-05-08 |
| Terminated | 2021-02-11 |
| Distributed | Nationwide (US) |
| Quantity | 111,492 canisters |
| Reason classes | labeling |
| Lot numbers | 12/21, 14049A |
Product
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-1280-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.