Product NDC: | 59088-852 |
Proprietary Name: | GenRx Cala Zinc Skin Healing |
Non Proprietary Name: | Zinc Oxide |
Active Ingredient(s): | 200 mg/mL & nbsp; Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | PASTE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59088-852 |
Labeler Name: | PureTek Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130108 |
Package NDC: | 59088-852-08 |
Package Description: | 118 mL in 1 TUBE (59088-852-08) |
NDC Code | 59088-852-08 |
Proprietary Name | GenRx Cala Zinc Skin Healing |
Package Description | 118 mL in 1 TUBE (59088-852-08) |
Product NDC | 59088-852 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Oxide |
Dosage Form Name | PASTE |
Route Name | TOPICAL |
Start Marketing Date | 20130108 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | PureTek Corporation |
Substance Name | ZINC OXIDE |
Strength Number | 200 |
Strength Unit | mg/mL |
Pharmaceutical Classes |