| 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 |