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 |