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 |