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Mineral Sunscreen SPF 20
Mineral Sunscreen SPF 20 - 10477-1538-1 - (Octinoxate, Octisalate, Zinc Oxide)
Drug Information of Mineral Sunscreen SPF 20
| 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) |
Labeler Information of Mineral Sunscreen SPF 20
| 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 Information of Mineral Sunscreen SPF 20
| Package NDC: | 10477-1538-1 |
| Package Description: | 50 g in 1 JAR (10477-1538-1) |
NDC Information of Mineral Sunscreen SPF 20
| NDC Code | 10477-1538-1 |
| Proprietary Name | Mineral Sunscreen SPF 20 |
| Package Description | 50 g in 1 JAR (10477-1538-1) |
| 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 |
