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DDF
DDF - 37000-721-17 - (Salicylic Acid)
Drug Information of DDF
| Product NDC: | 37000-721 |
| Proprietary Name: | DDF |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | .015 g/g & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DDF
| Product NDC: | 37000-721 |
| Labeler Name: | Procter & Gamble Manufacturing Co. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090601 |
Package Information of DDF
| Package NDC: | 37000-721-17 |
| Package Description: | 1 TUBE in 1 CARTON (37000-721-17) > 48 g in 1 TUBE |
NDC Information of DDF
| NDC Code | 37000-721-17 |
| Proprietary Name | DDF |
| Package Description | 1 TUBE in 1 CARTON (37000-721-17) > 48 g in 1 TUBE |
| Product NDC | 37000-721 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Co. |
| Substance Name | SALICYLIC ACID |
| Strength Number | .015 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
