Sodium Sulfacetamide 10% and Sulfur 5% Lotion — Class III drug recall D-602-2013
Terminated recall by Mission Pharmacal Co, reported 2013-06-26, distributed nationwide. Superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label
| Recall number | D-602-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mission Pharmacal Co, Boerne, TX, United States |
| Recall initiated | 2013-01-23 |
| Classified | 2013-06-14 |
| Reported by FDA | 2013-06-26 |
| Terminated | 2014-03-18 |
| Distributed | Nationwide (US) |
| Quantity | 8,437 bottles |
| Reason classes | labeling, potency |
| NDC | 42792-0102-01 |
| Lot numbers | 05/14, 09/14, E112, J062 |
Product
Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE
Reason for recall
Superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label strength.
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-602-2013. 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.