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DDF
DDF - 37000-724-01 - (Salicylic Acid)
Drug Information of DDF
| Product NDC: | 37000-724 |
| Proprietary Name: | DDF |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 17.64 mg/mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DDF
| Product NDC: | 37000-724 |
| Labeler Name: | Procter & Gamble Manufacturing Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100201 |
Package Information of DDF
| Package NDC: | 37000-724-01 |
| Package Description: | 50 mL in 1 TUBE (37000-724-01) |
NDC Information of DDF
| NDC Code | 37000-724-01 |
| Proprietary Name | DDF |
| Package Description | 50 mL in 1 TUBE (37000-724-01) |
| Product NDC | 37000-724 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20100201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Co. |
| Substance Name | SALICYLIC ACID |
| Strength Number | 17.64 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
