DLC Laboratories, Inc
FDA Regulatory Profile
DLC Laboratories, Inc appears in FDA public data with 2 recalls, 1 510(k) clearance, 8 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-0257-2021, Class II) was initiated on January 6, 2021. Its most recent 510(k) clearance was granted on December 4, 2006.
Summary
- Total Recalls
- 2
- 510(k) Clearances
- 1
- Inspections
- 8
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| D-0257-2021 | Class II | Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cru | January 6, 2021 |
| D-0241-2018 | Class II | Earth's Care Eczema Lotion (2% Colloidal Oatmeal) Skin Protectant with Aloe and Almond Oil, 8 fl. oz | December 28, 2017 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K061466 | INTIMOL | December 4, 2006 |