Product NDC: | 37000-701 |
Proprietary Name: | DDF Sulfur Therapeutic |
Non Proprietary Name: | sulfur |
Active Ingredient(s): | 100 mg/g & nbsp; sulfur |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 37000-701 |
Labeler Name: | Procter & Gamble Manufacturing Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333D |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130501 |
Package NDC: | 37000-701-11 |
Package Description: | 1 JAR in 1 CARTON (37000-701-11) > 113 g in 1 JAR |
NDC Code | 37000-701-11 |
Proprietary Name | DDF Sulfur Therapeutic |
Package Description | 1 JAR in 1 CARTON (37000-701-11) > 113 g in 1 JAR |
Product NDC | 37000-701 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | sulfur |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20130501 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Procter & Gamble Manufacturing Company |
Substance Name | SULFUR |
Strength Number | 100 |
Strength Unit | mg/g |
Pharmaceutical Classes |