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 |