Product NDC: | 49546-105 |
Proprietary Name: | Ivy-Dry Super |
Non Proprietary Name: | BENZYL ALCOHOL, CAMPHOR, MENTHOL |
Active Ingredient(s): | 10; .5; .25 mL/100mL; mL/100mL; mL/100mL & nbsp; BENZYL ALCOHOL, CAMPHOR, MENTHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49546-105 |
Labeler Name: | Ivy-Dry, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120711 |
Package NDC: | 49546-105-03 |
Package Description: | 89 mL in 1 CANISTER (49546-105-03) |
NDC Code | 49546-105-03 |
Proprietary Name | Ivy-Dry Super |
Package Description | 89 mL in 1 CANISTER (49546-105-03) |
Product NDC | 49546-105 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | BENZYL ALCOHOL, CAMPHOR, MENTHOL |
Dosage Form Name | SPRAY |
Route Name | TOPICAL |
Start Marketing Date | 20120711 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ivy-Dry, Inc. |
Substance Name | BENZYL ALCOHOL; CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | 10; .5; .25 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |