| Product NDC: | 50021-062 | 
| Proprietary Name: | SUNZONE FAMILY SPF 60 | 
| Non Proprietary Name: | Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. | 
| Active Ingredient(s): | 4.65; 18.6; 7.75; 7.75; 7.75; 9.3 g/155g; g/155g; g/155g; g/155g; g/155g; g/155g & nbsp; Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | AEROSOL, SPRAY | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 50021-062 | 
| Labeler Name: | Empack Spraytech Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part352 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20121116 | 
| Package NDC: | 50021-062-01 | 
| Package Description: | 155 g in 1 CAN (50021-062-01) | 
| NDC Code | 50021-062-01 | 
| Proprietary Name | SUNZONE FAMILY SPF 60 | 
| Package Description | 155 g in 1 CAN (50021-062-01) | 
| Product NDC | 50021-062 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Octinoxate, Octocrylene, Octisalate, Oxybenzone, Avobenzone and Homosalate. | 
| Dosage Form Name | AEROSOL, SPRAY | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20121116 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Empack Spraytech Inc. | 
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE | 
| Strength Number | 4.65; 18.6; 7.75; 7.75; 7.75; 9.3 | 
| Strength Unit | g/155g; g/155g; g/155g; g/155g; g/155g; g/155g | 
| Pharmaceutical Classes |