Product NDC: | 75916-3025 |
Proprietary Name: | SurfersSkin Face Sunscreen |
Non Proprietary Name: | OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
Active Ingredient(s): | 6; 3.3; 14.25 g/100g; g/100g; g/100g & nbsp; OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75916-3025 |
Labeler Name: | Skin Alive, Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110127 |
Package NDC: | 75916-3025-1 |
Package Description: | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-3025-1) > 40 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 75916-3025-1 |
Proprietary Name | SurfersSkin Face Sunscreen |
Package Description | 1 TUBE, WITH APPLICATOR in 1 BOX (75916-3025-1) > 40 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 75916-3025 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20110127 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Skin Alive, Ltd. |
Substance Name | OCTOCRYLENE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 6; 3.3; 14.25 |
Strength Unit | g/100g; g/100g; g/100g |
Pharmaceutical Classes |