| Product NDC: | 62839-1133 |
| Proprietary Name: | Sunright BodyBlock SPF15 |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Active Ingredient(s): | 20; 75; 30; 30 g/1000mL; g/1000mL; g/1000mL; g/1000mL & nbsp; Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62839-1133 |
| Labeler Name: | NSE Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100901 |
| Package NDC: | 62839-1133-1 |
| Package Description: | 100 mL in 1 TUBE (62839-1133-1) |
| NDC Code | 62839-1133-1 |
| Proprietary Name | Sunright BodyBlock SPF15 |
| Package Description | 100 mL in 1 TUBE (62839-1133-1) |
| Product NDC | 62839-1133 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octisalate, and Oxybenzone |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | NSE Products, Inc. |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
| Strength Number | 20; 75; 30; 30 |
| Strength Unit | g/1000mL; g/1000mL; g/1000mL; g/1000mL |
| Pharmaceutical Classes |