Home
>
National Drug Code (NDC)
>
Stridex
Stridex - 10157-1010-3 - (Salicylic Acid)
Drug Information of Stridex
| Product NDC: | 10157-1010 |
| Proprietary Name: | Stridex |
| Non Proprietary Name: | Salicylic Acid |
| Active Ingredient(s): | 1 g/100mL & nbsp; Salicylic Acid |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Stridex
| Product NDC: | 10157-1010 |
| Labeler Name: | Blistex Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333D |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of Stridex
| Package NDC: | 10157-1010-3 |
| Package Description: | 90 APPLICATOR in 1 JAR (10157-1010-3) > 2 mL in 1 APPLICATOR |
NDC Information of Stridex
| NDC Code | 10157-1010-3 |
| Proprietary Name | Stridex |
| Package Description | 90 APPLICATOR in 1 JAR (10157-1010-3) > 2 mL in 1 APPLICATOR |
| Product NDC | 10157-1010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Salicylic Acid |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blistex Inc |
| Substance Name | SALICYLIC ACID |
| Strength Number | 1 |
| Strength Unit | g/100mL |
| Pharmaceutical Classes |
