FDA Drug recall D-602-2013
Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE
- FDA Drug
- Class III
- terminated
- Published 2013-06-26
On 2013-06-26 the FDA classified a Class III recall of Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE by Mission Pharmacal, citing superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label strength.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-602-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-01-23 |
| Published | 2013-06-26 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Mission Pharmacal |
| Distribution | US |
Product
Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE
Reason
Superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label strength.
Identifiers
| code_info | Lot# E112, Exp 05/14 Lot# J062, Exp 09/14 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-602-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.