Product NDC: | 63509-002 |
Proprietary Name: | Skin Activator |
Non Proprietary Name: | Octinoxate, Octisalate and Avobenzone |
Active Ingredient(s): | .0142; .0661; .0472 g/mL; g/mL; g/mL & nbsp; Octinoxate, Octisalate and Avobenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63509-002 |
Labeler Name: | Cosmint Spa. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111021 |
Package NDC: | 63509-002-01 |
Package Description: | 1 TUBE in 1 CARTON (63509-002-01) > 15 mL in 1 TUBE |
NDC Code | 63509-002-01 |
Proprietary Name | Skin Activator |
Package Description | 1 TUBE in 1 CARTON (63509-002-01) > 15 mL in 1 TUBE |
Product NDC | 63509-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Octinoxate, Octisalate and Avobenzone |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20111021 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cosmint Spa. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | .0142; .0661; .0472 |
Strength Unit | g/mL; g/mL; g/mL |
Pharmaceutical Classes |