Product NDC: | 49546-201 |
Proprietary Name: | Ivy Dry |
Non Proprietary Name: | Benzyl Alcohol, Camphor, Menthol |
Active Ingredient(s): | 10; .6; .4 g/100g; g/100g; g/100g & nbsp; Benzyl Alcohol, Camphor, Menthol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49546-201 |
Labeler Name: | Ivy Dry, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part348 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120822 |
Package NDC: | 49546-201-28 |
Package Description: | 1 TUBE in 1 BOX (49546-201-28) > 28 g in 1 TUBE |
NDC Code | 49546-201-28 |
Proprietary Name | Ivy Dry |
Package Description | 1 TUBE in 1 BOX (49546-201-28) > 28 g in 1 TUBE |
Product NDC | 49546-201 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzyl Alcohol, Camphor, Menthol |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120822 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Ivy Dry, Inc. |
Substance Name | BENZYL ALCOHOL; CAMPHOR (SYNTHETIC); MENTHOL |
Strength Number | 10; .6; .4 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |