| Product NDC: | 65643-336 |
| Proprietary Name: | Bellagio Childrens Sunscreen SPF 45 |
| Non Proprietary Name: | Homosalate, Octinoxate, Octisalate, Oxybenzone, and Zinc Oxide |
| Active Ingredient(s): | 141.904; 65.884; 50.68; 50.68; 27.773 mg/mL; mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Homosalate, Octinoxate, Octisalate, Oxybenzone, and Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 65643-336 |
| Labeler Name: | Lifetech Resources, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090201 |
| Package NDC: | 65643-336-19 |
| Package Description: | 118 mL in 1 TUBE (65643-336-19) |
| NDC Code | 65643-336-19 |
| Proprietary Name | Bellagio Childrens Sunscreen SPF 45 |
| Package Description | 118 mL in 1 TUBE (65643-336-19) |
| Product NDC | 65643-336 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Homosalate, Octinoxate, Octisalate, Oxybenzone, and Zinc Oxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090201 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Lifetech Resources, LLC |
| Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 141.904; 65.884; 50.68; 50.68; 27.773 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |