| 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: | 63736-363-05 |
| Package Description: | 142 g in 1 BOTTLE, DISPENSING (63736-363-05) |
| NDC Code | 63736-363-05 |
| Proprietary Name | Caldesene |
| Package Description | 142 g in 1 BOTTLE, DISPENSING (63736-363-05) |
| 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 |