| Product NDC: | 76159-124 |
| Proprietary Name: | 3LAB Hydra Day SPF 20 Broad Spectrum Water-Based Sunscreen |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, AVOBENZONE |
| Active Ingredient(s): | 2; 75; 46 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE, AVOBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 76159-124 |
| Labeler Name: | 3LAB, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121015 |
| Package NDC: | 76159-124-01 |
| Package Description: | 60 mL in 1 BOTTLE (76159-124-01) |
| NDC Code | 76159-124-01 |
| Proprietary Name | 3LAB Hydra Day SPF 20 Broad Spectrum Water-Based Sunscreen |
| Package Description | 60 mL in 1 BOTTLE (76159-124-01) |
| Product NDC | 76159-124 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, AVOBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121015 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | 3LAB, Inc |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
| Strength Number | 2; 75; 46 |
| Strength Unit | mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |