Product NDC: | 10477-1538 |
Proprietary Name: | Mineral Sunscreen SPF 20 |
Non Proprietary Name: | Octinoxate, Octisalate, Zinc Oxide |
Active Ingredient(s): | 3; 2; 5 g/100g; g/100g; g/100g & nbsp; Octinoxate, Octisalate, Zinc Oxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10477-1538 |
Labeler Name: | Goodier Cosmetics, LP |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050906 |
Package NDC: | 10477-1538-2 |
Package Description: | 1 JAR in 1 CARTON (10477-1538-2) > 48 g in 1 JAR |
NDC Code | 10477-1538-2 |
Proprietary Name | Mineral Sunscreen SPF 20 |
Package Description | 1 JAR in 1 CARTON (10477-1538-2) > 48 g in 1 JAR |
Product NDC | 10477-1538 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate, Zinc Oxide |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20050906 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Goodier Cosmetics, LP |
Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
Strength Number | 3; 2; 5 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |