Product NDC: | 68026-542 |
Proprietary Name: | Anti-Aging Hydra Tint SPF 20 Shade 20 |
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: | 68026-542 |
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: | 68026-542-40 |
Package Description: | 1 BOTTLE in 1 CARTON (68026-542-40) > 40 mL in 1 BOTTLE |
NDC Code | 68026-542-40 |
Proprietary Name | Anti-Aging Hydra Tint SPF 20 Shade 20 |
Package Description | 1 BOTTLE in 1 CARTON (68026-542-40) > 40 mL in 1 BOTTLE |
Product NDC | 68026-542 |
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 |