Product NDC: | 57913-2869 |
Proprietary Name: | Hydraphel Day SPF15 |
Non Proprietary Name: | Avobenzone and Octinoxate |
Active Ingredient(s): | 20; 75 mg/mL; mg/mL & nbsp; Avobenzone and Octinoxate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 57913-2869 |
Labeler Name: | Erno Laszlo, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130410 |
Package NDC: | 57913-2869-9 |
Package Description: | 1 JAR in 1 CARTON (57913-2869-9) > 50 mL in 1 JAR |
NDC Code | 57913-2869-9 |
Proprietary Name | Hydraphel Day SPF15 |
Package Description | 1 JAR in 1 CARTON (57913-2869-9) > 50 mL in 1 JAR |
Product NDC | 57913-2869 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone and Octinoxate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20130410 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Erno Laszlo, Inc. |
Substance Name | AVOBENZONE; OCTINOXATE |
Strength Number | 20; 75 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |