| Product NDC: | 62742-4056 |
| Proprietary Name: | Moisturizing Face Screen SPF 30 |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 200 mg/mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62742-4056 |
| Labeler Name: | Allure Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100901 |
| Package NDC: | 62742-4056-1 |
| Package Description: | 60 mL in 1 BOTTLE, PUMP (62742-4056-1) |
| NDC Code | 62742-4056-1 |
| Proprietary Name | Moisturizing Face Screen SPF 30 |
| Package Description | 60 mL in 1 BOTTLE, PUMP (62742-4056-1) |
| Product NDC | 62742-4056 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Allure Labs, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 200 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |