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DDF Sulfur Therapeutic
DDF Sulfur Therapeutic - 37000-701-11 - (sulfur)
Drug Information of DDF Sulfur Therapeutic
| 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) |
Labeler Information of DDF Sulfur Therapeutic
| 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 Information of DDF Sulfur Therapeutic
| Package NDC: | 37000-701-11 |
| Package Description: | 1 JAR in 1 CARTON (37000-701-11) > 113 g in 1 JAR |
NDC Information of DDF Sulfur Therapeutic
| 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 |
