| Product NDC: | 76230-727 |
| Proprietary Name: | Everyday Facial Moisturizer And Sunscreen SPF 20 |
| Non Proprietary Name: | ZINC OXIDE |
| Active Ingredient(s): | 16.32 mL/100mL & nbsp; ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76230-727 |
| Labeler Name: | 714 Essentials LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110609 |
| Package NDC: | 76230-727-09 |
| Package Description: | 1 BOTTLE in 1 PACKAGE (76230-727-09) > 75 mL in 1 BOTTLE |
| NDC Code | 76230-727-09 |
| Proprietary Name | Everyday Facial Moisturizer And Sunscreen SPF 20 |
| Package Description | 1 BOTTLE in 1 PACKAGE (76230-727-09) > 75 mL in 1 BOTTLE |
| Product NDC | 76230-727 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110609 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | 714 Essentials LTD |
| Substance Name | ZINC OXIDE |
| Strength Number | 16.32 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |