| Product NDC: | 50021-508 |
| Proprietary Name: | SunZone Sunscreen Family SPF 30 |
| Non Proprietary Name: | Octinoxate and Avobenzone |
| Active Ingredient(s): | 1.76; 4.7 g/235g; g/235g & nbsp; Octinoxate and Avobenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50021-508 |
| Labeler Name: | Empack Spraytech Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130102 |
| Package NDC: | 50021-508-01 |
| Package Description: | 235 g in 1 TUBE (50021-508-01) |
| NDC Code | 50021-508-01 |
| Proprietary Name | SunZone Sunscreen Family SPF 30 |
| Package Description | 235 g in 1 TUBE (50021-508-01) |
| Product NDC | 50021-508 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate and Avobenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130102 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Empack Spraytech Inc |
| Substance Name | AVOBENZONE; OCTINOXATE |
| Strength Number | 1.76; 4.7 |
| Strength Unit | g/235g; g/235g |
| Pharmaceutical Classes |