Product NDC: | 66097-003 |
Proprietary Name: | Sunleya Age Minimizing Sun Care |
Non Proprietary Name: | AVOBENZONE, HOMOSALTE, OCTISALATE, OCTOCRYLENE |
Active Ingredient(s): | 30; 150; 50; 100 mg/g; mg/g; mg/g; mg/g & nbsp; AVOBENZONE, HOMOSALTE, OCTISALATE, OCTOCRYLENE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66097-003 |
Labeler Name: | C.F.E.B. Sisley |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130121 |
Package NDC: | 66097-003-51 |
Package Description: | 1 BOTTLE in 1 BOX (66097-003-51) > 51.5 g in 1 BOTTLE |
NDC Code | 66097-003-51 |
Proprietary Name | Sunleya Age Minimizing Sun Care |
Package Description | 1 BOTTLE in 1 BOX (66097-003-51) > 51.5 g in 1 BOTTLE |
Product NDC | 66097-003 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE, HOMOSALTE, OCTISALATE, OCTOCRYLENE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130121 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | C.F.E.B. Sisley |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE |
Strength Number | 30; 150; 50; 100 |
Strength Unit | mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |