| Product NDC: | 65643-329 |
| Proprietary Name: | Bellagio Sunscreen SPF 30 |
| Non Proprietary Name: | Octinoxate, Octocrylene, Oxybenzone, and Octisalate |
| Active Ingredient(s): | 68.32; 48.8; 68.32; 58.56 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Octinoxate, Octocrylene, Oxybenzone, and Octisalate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SPRAY |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65643-329 |
| Labeler Name: | Lifetech Resources, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090101 |
| Package NDC: | 65643-329-11 |
| Package Description: | 237 mL in 1 BOTTLE, SPRAY (65643-329-11) |
| NDC Code | 65643-329-11 |
| Proprietary Name | Bellagio Sunscreen SPF 30 |
| Package Description | 237 mL in 1 BOTTLE, SPRAY (65643-329-11) |
| Product NDC | 65643-329 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Octinoxate, Octocrylene, Oxybenzone, and Octisalate |
| Dosage Form Name | SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20090101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Lifetech Resources, LLC |
| Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
| Strength Number | 68.32; 48.8; 68.32; 58.56 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |