Product NDC: | 75934-0003 |
Proprietary Name: | Skin Protectant |
Non Proprietary Name: | zinc oxide, dimethicone |
Active Ingredient(s): | 20; 120 mg/g; mg/g & nbsp; zinc oxide, dimethicone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75934-0003 |
Labeler Name: | Tiger Medical Group (US), Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part347 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 75934-0003-2 |
Package Description: | 113.6 g in 1 TUBE (75934-0003-2) |
NDC Code | 75934-0003-2 |
Proprietary Name | Skin Protectant |
Package Description | 113.6 g in 1 TUBE (75934-0003-2) |
Product NDC | 75934-0003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | zinc oxide, dimethicone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Tiger Medical Group (US), Inc. |
Substance Name | DIMETHICONE; ZINC OXIDE |
Strength Number | 20; 120 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes |