| Product NDC: | 52960-201 |
| Proprietary Name: | iBlanc Restora-Bright Elite Natural Sun Defense |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 13.5 g/100g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 52960-201 |
| Labeler Name: | iBlanc, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120923 |
| Package NDC: | 52960-201-12 |
| Package Description: | 45 g in 1 TUBE (52960-201-12) |
| NDC Code | 52960-201-12 |
| Proprietary Name | iBlanc Restora-Bright Elite Natural Sun Defense |
| Package Description | 45 g in 1 TUBE (52960-201-12) |
| Product NDC | 52960-201 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120923 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | iBlanc, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 13.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |