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 |