| Product NDC: | 10477-2627 |
| Proprietary Name: | Tinted SPF 45 |
| Non Proprietary Name: | Octinoxate, Octisalate, Zinc Oxide |
| Active Ingredient(s): | 7.5; 5; 2 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: | 10477-2627 |
| Labeler Name: | Goodier Cosmetics, LP |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20071201 |
| Package NDC: | 10477-2627-3 |
| Package Description: | 3 g in 1 TUBE (10477-2627-3) |
| NDC Code | 10477-2627-3 |
| Proprietary Name | Tinted SPF 45 |
| Package Description | 3 g in 1 TUBE (10477-2627-3) |
| Product NDC | 10477-2627 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octisalate, Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20071201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Goodier Cosmetics, LP |
| Substance Name | OCTINOXATE; OCTISALATE; ZINC OXIDE |
| Strength Number | 7.5; 5; 2 |
| Strength Unit | g/100g; g/100g; g/100g |
| Pharmaceutical Classes |