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 |