Product NDC: | 11523-0635 |
Proprietary Name: | DuoFilm Wart Remover |
Non Proprietary Name: | Salicylic Acid |
Active Ingredient(s): | 150.28 mg/mL & nbsp; Salicylic Acid |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11523-0635 |
Labeler Name: | MSD Consumer Care, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part358B |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19900814 |
Package NDC: | 11523-0635-2 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (11523-0635-2) > 9.8 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 11523-0635-2 |
Proprietary Name | DuoFilm Wart Remover |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (11523-0635-2) > 9.8 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 11523-0635 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Salicylic Acid |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19900814 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | MSD Consumer Care, Inc. |
Substance Name | SALICYLIC ACID |
Strength Number | 150.28 |
Strength Unit | mg/mL |
Pharmaceutical Classes |