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STRIDEX
STRIDEX - 10157-1070-1 - (Stridex naturally clear)
Drug Information of STRIDEX
| Product NDC: | 10157-1070 |
| Proprietary Name: | STRIDEX |
| Non Proprietary Name: | Stridex naturally clear |
| Active Ingredient(s): | .1 g/1 & nbsp; Stridex naturally clear |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of STRIDEX
| Product NDC: | 10157-1070 |
| Labeler Name: | Blistex inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20091123 |
Package Information of STRIDEX
| Package NDC: | 10157-1070-1 |
| Package Description: | 70 LIQUID in 1 JAR (10157-1070-1) |
NDC Information of STRIDEX
| NDC Code | 10157-1070-1 |
| Proprietary Name | STRIDEX |
| Package Description | 70 LIQUID in 1 JAR (10157-1070-1) |
| Product NDC | 10157-1070 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Stridex naturally clear |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20091123 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blistex inc |
| Substance Name | SALICYLIC ACID |
| Strength Number | .1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes |
