Product NDC: | 42263-101 |
Proprietary Name: | BABY SUNSCREEN |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 20 g/100g & nbsp; ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42263-101 |
Labeler Name: | SEVENTH GENERATION INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111230 |
Package NDC: | 42263-101-13 |
Package Description: | 85 g in 1 TUBE (42263-101-13) |
NDC Code | 42263-101-13 |
Proprietary Name | BABY SUNSCREEN |
Package Description | 85 g in 1 TUBE (42263-101-13) |
Product NDC | 42263-101 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20111230 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SEVENTH GENERATION INC |
Substance Name | ZINC OXIDE |
Strength Number | 20 |
Strength Unit | g/100g |
Pharmaceutical Classes |