Product NDC: | 37000-303 |
Proprietary Name: | Olay Professional |
Non Proprietary Name: | Sulfur |
Active Ingredient(s): | 120 mg/mL & nbsp; Sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-303 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110331 |
Package NDC: | 37000-303-50 |
Package Description: | 1 TUBE in 1 CARTON (37000-303-50) > 50 mL in 1 TUBE |
NDC Code | 37000-303-50 |
Proprietary Name | Olay Professional |
Package Description | 1 TUBE in 1 CARTON (37000-303-50) > 50 mL in 1 TUBE |
Product NDC | 37000-303 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Sulfur |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20110331 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | SULFUR |
Strength Number | 120 |
Strength Unit | mg/mL |
Pharmaceutical Classes |