Product NDC: | 63736-363 |
Proprietary Name: | Caldesene |
Non Proprietary Name: | Talc and Zinc Oxide |
Active Ingredient(s): | 57.51; 10.65 g/71g; g/71g & nbsp; Talc and Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-363 |
Labeler Name: | Insight Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20090709 |
Package NDC: | 63736-363-03 |
Package Description: | 71 g in 1 BOTTLE, DISPENSING (63736-363-03) |
NDC Code | 63736-363-03 |
Proprietary Name | Caldesene |
Package Description | 71 g in 1 BOTTLE, DISPENSING (63736-363-03) |
Product NDC | 63736-363 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Talc and Zinc Oxide |
Dosage Form Name | POWDER |
Route Name | TOPICAL |
Start Marketing Date | 20090709 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Insight Pharmaceuticals |
Substance Name | TALC; ZINC OXIDE |
Strength Number | 57.51; 10.65 |
Strength Unit | g/71g; g/71g |
Pharmaceutical Classes |