Product NDC: | 76041-713 |
Proprietary Name: | Wild Rose Daily Moisture Sunscreen |
Non Proprietary Name: | ZINC OXIDE |
Active Ingredient(s): | 19 mL/100mL & nbsp; ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 76041-713 |
Labeler Name: | Neal's Yard (Natural Remedies) Limited |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110610 |
Package NDC: | 76041-713-50 |
Package Description: | 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE |
NDC Code | 76041-713-50 |
Proprietary Name | Wild Rose Daily Moisture Sunscreen |
Package Description | 1 BOTTLE in 1 CARTON (76041-713-50) > 50 mL in 1 BOTTLE |
Product NDC | 76041-713 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110610 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Neal's Yard (Natural Remedies) Limited |
Substance Name | ZINC OXIDE |
Strength Number | 19 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |