| Product NDC: | 64768-2920 |
| Proprietary Name: | Mustela SPF 50 |
| Non Proprietary Name: | TITANIUM DIOXIDE and ZINC OXIDE |
| Active Ingredient(s): | 60; 47 mg/mL; mg/mL & nbsp; TITANIUM DIOXIDE and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 64768-2920 |
| Labeler Name: | Expanscience Laboratories d/b/a Mustela |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130215 |
| Package NDC: | 64768-2920-1 |
| Package Description: | 1 TUBE in 1 CARTON (64768-2920-1) > 100 mL in 1 TUBE |
| NDC Code | 64768-2920-1 |
| Proprietary Name | Mustela SPF 50 |
| Package Description | 1 TUBE in 1 CARTON (64768-2920-1) > 100 mL in 1 TUBE |
| Product NDC | 64768-2920 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TITANIUM DIOXIDE and ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130215 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Expanscience Laboratories d/b/a Mustela |
| Substance Name | TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | 60; 47 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes |