| 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 |