Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts
Class III · Low risk Terminated Initiated Jan 23, 2013 (14 years ago)

Sodium Sulfacetamide 10% and Sulfur 5% Lotion

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Superpotent: Drug product active ingredients were formulated incorrectly (too high) with respect to the label strength.

Cause type: Wrong potency / content

Sub- or super-potent product, or a failed content-uniformity / assay test. You may receive too little or too much active ingredient - a direct dosing risk. All wrong potency / content recalls.

What was recalled

Sodium Sulfacetamide 10% and Sulfur 5% Lotion, (NDC 42792-102-01), 25 g Manufactured for: Austin Pharmaceuticals, LLC, Wilmington, DE

Affected NDC 42792-0102-01

Compare with the code on your package — it is the most precise check available.

Drug: Sulfur

Recalling firm
Mission Pharmacal Co
NDC code
42792-102-01
Origin
TX, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-602-2013 · FDA notice

Low risk, still worth a check. Class III means the product is unlikely to cause harm but breaks an FDA rule (often labeling). If your lot matches, your pharmacy will normally swap it; there is no need for alarm. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other Sulfur recalls

See all

Other recalls by Mission Pharmacal Co

All 2013 recalls