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DDF
DDF - 37000-700-48 - (Salicylic Acid)
Drug Information of DDF
| Product NDC: | 37000-700 |
| Proprietary Name: | DDF |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 100 mg/g & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DDF
| Product NDC: | 37000-700 |
| Labeler Name: | Procter & Gamble Manufacturing Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120101 |
Package Information of DDF
| Package NDC: | 37000-700-48 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (37000-700-48) > 48 g in 1 BOTTLE, PUMP |
NDC Information of DDF
| NDC Code | 37000-700-48 |
| Proprietary Name | DDF |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (37000-700-48) > 48 g in 1 BOTTLE, PUMP |
| Product NDC | 37000-700 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20120101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Procter & Gamble Manufacturing Company |
| Substance Name | SALICYLIC ACID |
| Strength Number | 100 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
