| Product NDC: | 68026-341 |
| Proprietary Name: | White Caviar Illuminating Hand SPF 15 |
| Non Proprietary Name: | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Active Ingredient(s): | 3; 5; 4; 3; 1.5 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68026-341 |
| Labeler Name: | La Prairie, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111006 |
| Package NDC: | 68026-341-15 |
| Package Description: | 1 TUBE in 1 CARTON (68026-341-15) > 15 mL in 1 TUBE |
| NDC Code | 68026-341-15 |
| Proprietary Name | White Caviar Illuminating Hand SPF 15 |
| Package Description | 1 TUBE in 1 CARTON (68026-341-15) > 15 mL in 1 TUBE |
| Product NDC | 68026-341 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OCTOCRYLENE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20111006 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | La Prairie, Inc. |
| Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 3; 5; 4; 3; 1.5 |
| Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
| Pharmaceutical Classes |