| Product NDC: | 50021-307 |
| Proprietary Name: | SunZone Sunscreen Family SPF 30 |
| Non Proprietary Name: | Octisalate, Oxybenzone, Avobenzone and Homosalate. |
| Active Ingredient(s): | 3.02; 22.65; 7.55; 6.04 g/151g; g/151g; g/151g; g/151g & nbsp; Octisalate, Oxybenzone, Avobenzone and Homosalate. |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50021-307 |
| 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: | 50021-307-01 |
| Package Description: | 151 g in 1 CAN (50021-307-01) |
| NDC Code | 50021-307-01 |
| Proprietary Name | SunZone Sunscreen Family SPF 30 |
| Package Description | 151 g in 1 CAN (50021-307-01) |
| Product NDC | 50021-307 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | 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; OCTISALATE; OXYBENZONE |
| Strength Number | 3.02; 22.65; 7.55; 6.04 |
| Strength Unit | g/151g; g/151g; g/151g; g/151g |
| Pharmaceutical Classes |