| Product NDC: | 66915-611 |
| Proprietary Name: | Daytime Defense SPF 30 |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | .135 mg/g & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66915-611 |
| Labeler Name: | CoValence, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20120426 |
| Package NDC: | 66915-611-01 |
| Package Description: | 200000 g in 1 DRUM (66915-611-01) |
| NDC Code | 66915-611-01 |
| Proprietary Name | Daytime Defense SPF 30 |
| Package Description | 200000 g in 1 DRUM (66915-611-01) |
| Product NDC | 66915-611 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120426 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CoValence, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | .135 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |