| Product NDC: | 24286-1525 |
| Proprietary Name: | De La Cruz Sulfur Acne Medication |
| Non Proprietary Name: | SULFUR |
| Active Ingredient(s): | 10 g/100g & nbsp; SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 24286-1525 |
| Labeler Name: | DLC Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120727 |
| Package NDC: | 24286-1525-2 |
| Package Description: | 73.7 g in 1 JAR (24286-1525-2) |
| NDC Code | 24286-1525-2 |
| Proprietary Name | De La Cruz Sulfur Acne Medication |
| Package Description | 73.7 g in 1 JAR (24286-1525-2) |
| Product NDC | 24286-1525 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | SULFUR |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120727 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | DLC Laboratories, Inc. |
| Substance Name | SULFUR |
| Strength Number | 10 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |