Product NDC: | 53698-001 |
Proprietary Name: | Premium Sunscreen Broad Spectrum SPF 30 |
Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
Active Ingredient(s): | 30; 100; 50; 60 mg/100mL; mg/100mL; mg/100mL; mg/100mL & nbsp; AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53698-001 |
Labeler Name: | Pro Sun Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20121010 |
Package NDC: | 53698-001-00 |
Package Description: | 100 mL in 1 TUBE (53698-001-00) |
NDC Code | 53698-001-00 |
Proprietary Name | Premium Sunscreen Broad Spectrum SPF 30 |
Package Description | 100 mL in 1 TUBE (53698-001-00) |
Product NDC | 53698-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20121010 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Pro Sun Products |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 30; 100; 50; 60 |
Strength Unit | mg/100mL; mg/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes |