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SUN Solar Defense Hydrating
SUN Solar Defense Hydrating - 62742-4037-1 - (Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate)
Drug Information of SUN Solar Defense Hydrating
| Product NDC: | 62742-4037 |
| Proprietary Name: | SUN Solar Defense Hydrating |
| Non Proprietary Name: | Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate |
| Active Ingredient(s): | 75; 50; 30; 50 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SUN Solar Defense Hydrating
| Product NDC: | 62742-4037 |
| Labeler Name: | Allure Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100101 |
Package Information of SUN Solar Defense Hydrating
| Package NDC: | 62742-4037-1 |
| Package Description: | 118 mL in 1 TUBE (62742-4037-1) |
NDC Information of SUN Solar Defense Hydrating
| NDC Code | 62742-4037-1 |
| Proprietary Name | SUN Solar Defense Hydrating |
| Package Description | 118 mL in 1 TUBE (62742-4037-1) |
| Product NDC | 62742-4037 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Zinc Oxide, Ethylhexyl Methoxycinnamate, Benzophenone, Ethylhexyl Salicylate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Allure Labs, Inc. |
| Substance Name | OCTINOXATE; OCTISALATE; OXYBENZONE; ZINC OXIDE |
| Strength Number | 75; 50; 30; 50 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |
