| Product NDC: | 67402-051 |
| Proprietary Name: | Environmental Defense Sunscreen SPF 50 |
| Non Proprietary Name: | Octinoxate, Oxybenzone, Octisalate, Zinc oxide, Octocrylene |
| Active Ingredient(s): | 75; 50; 2; 60; 3.3 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Octinoxate, Oxybenzone, Octisalate, Zinc oxide, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67402-051 |
| Labeler Name: | Skinmedica Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100428 |
| Package NDC: | 67402-051-13 |
| Package Description: | 12 TUBE in 1 BOX (67402-051-13) > 3.7 g in 1 TUBE |
| NDC Code | 67402-051-13 |
| Proprietary Name | Environmental Defense Sunscreen SPF 50 |
| Package Description | 12 TUBE in 1 BOX (67402-051-13) > 3.7 g in 1 TUBE |
| Product NDC | 67402-051 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Oxybenzone, Octisalate, Zinc oxide, Octocrylene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100428 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skinmedica Inc |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 75; 50; 2; 60; 3.3 |
| Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
| Pharmaceutical Classes |