Product NDC: | 10096-0306 |
Proprietary Name: | Magix |
Non Proprietary Name: | OCTINOXATE, OCTISALATE |
Active Ingredient(s): | 75; 40 mg/mL; mg/mL & nbsp; OCTINOXATE, OCTISALATE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10096-0306 |
Labeler Name: | Avon Products, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20130530 |
Package NDC: | 10096-0306-2 |
Package Description: | 1 TUBE in 1 CARTON (10096-0306-2) > 30 mL in 1 TUBE (10096-0306-1) |
NDC Code | 10096-0306-2 |
Proprietary Name | Magix |
Package Description | 1 TUBE in 1 CARTON (10096-0306-2) > 30 mL in 1 TUBE (10096-0306-1) |
Product NDC | 10096-0306 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130530 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Avon Products, Inc |
Substance Name | OCTINOXATE; OCTISALATE |
Strength Number | 75; 40 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |