| Product NDC: | 68026-541 |
| Proprietary Name: | Anti-Aging Hydra Tint SPF 20 Shade 10 |
| Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
| Active Ingredient(s): | 7.5; 3.5 mL/100mL; mL/100mL & nbsp; OCTINOXATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68026-541 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111010 |
| Package NDC: | 68026-541-40 |
| Package Description: | 1 BOTTLE in 1 CARTON (68026-541-40) > 40 mL in 1 BOTTLE |
| NDC Code | 68026-541-40 |
| Proprietary Name | Anti-Aging Hydra Tint SPF 20 Shade 10 |
| Package Description | 1 BOTTLE in 1 CARTON (68026-541-40) > 40 mL in 1 BOTTLE |
| Product NDC | 68026-541 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111010 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7.5; 3.5 |
| Strength Unit | mL/100mL; mL/100mL |
| Pharmaceutical Classes |