| Product NDC: | 62742-4040 |
| Proprietary Name: | SUN Solar Defense Oil-free SPF 30 |
| Non Proprietary Name: | Zinc Oxide |
| Active Ingredient(s): | 186 mg/mL & nbsp; Zinc Oxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 62742-4040 |
| Labeler Name: | Allure Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
| Package NDC: | 62742-4040-1 |
| Package Description: | 118 mL in 1 TUBE (62742-4040-1) |
| NDC Code | 62742-4040-1 |
| Proprietary Name | SUN Solar Defense Oil-free SPF 30 |
| Package Description | 118 mL in 1 TUBE (62742-4040-1) |
| Product NDC | 62742-4040 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allure Labs, Inc. |
| Substance Name | ZINC OXIDE |
| Strength Number | 186 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |