Product NDC: | 59663-140 |
Proprietary Name: | Bella Pelle SPF 30 |
Non Proprietary Name: | OCTINOXATE, ZINC OXIDE |
Active Ingredient(s): | 75; 100 mg/mL; mg/mL & nbsp; OCTINOXATE, ZINC OXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59663-140 |
Labeler Name: | Shine & Pretty (USA), Corp. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130301 |
Package NDC: | 59663-140-04 |
Package Description: | 120 mL in 1 TUBE (59663-140-04) |
NDC Code | 59663-140-04 |
Proprietary Name | Bella Pelle SPF 30 |
Package Description | 120 mL in 1 TUBE (59663-140-04) |
Product NDC | 59663-140 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, ZINC OXIDE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130301 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Shine & Pretty (USA), Corp. |
Substance Name | OCTINOXATE; ZINC OXIDE |
Strength Number | 75; 100 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |