| Product NDC: | 75916-4020 |
| Proprietary Name: | Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Active Ingredient(s): | 75; 34.5; 10; 19.5 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 75916-4020 |
| Labeler Name: | Skin Alive, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110131 |
| Package NDC: | 75916-4020-5 |
| Package Description: | 2000 mL in 1 BOTTLE (75916-4020-5) |
| NDC Code | 75916-4020-5 |
| Proprietary Name | Golfers Skin Broad Spectrum SPF 30 Plus Sunscreen |
| Package Description | 2000 mL in 1 BOTTLE (75916-4020-5) |
| Product NDC | 75916-4020 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE, TITANIUM DIOXIDE, ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110131 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skin Alive, Ltd. |
| Substance Name | OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 75; 34.5; 10; 19.5 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |