Product NDC: | 44099-001 |
Proprietary Name: | skin MD Natural |
Non Proprietary Name: | octinoxate, octisalate, homosalate |
Active Ingredient(s): | 3; 7; 5 mg/100mL; mg/100mL; mg/100mL & nbsp; octinoxate, octisalate, homosalate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44099-001 |
Labeler Name: | 21st Century Formulations |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080819 |
Package NDC: | 44099-001-02 |
Package Description: | 236 mL in 1 BOTTLE (44099-001-02) |
NDC Code | 44099-001-02 |
Proprietary Name | skin MD Natural |
Package Description | 236 mL in 1 BOTTLE (44099-001-02) |
Product NDC | 44099-001 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octinoxate, octisalate, homosalate |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20080819 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | 21st Century Formulations |
Substance Name | HOMOSALATE; OCTINOXATE; OCTISALATE |
Strength Number | 3; 7; 5 |
Strength Unit | mg/100mL; mg/100mL; mg/100mL |
Pharmaceutical Classes |