| Product NDC: | 11045-0303 |
| Proprietary Name: | Soleo Organics Sunscreen |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 223 mg/g & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11045-0303 |
| Labeler Name: | Skin Elements USA, LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20070120 |
| Package NDC: | 11045-0303-2 |
| Package Description: | 80 g in 1 TUBE (11045-0303-2) |
| NDC Code | 11045-0303-2 |
| Proprietary Name | Soleo Organics Sunscreen |
| Package Description | 80 g in 1 TUBE (11045-0303-2) |
| Product NDC | 11045-0303 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070120 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Skin Elements USA, LLC |
| Substance Name | ZINC OXIDE |
| Strength Number | 223 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |