Product NDC: | 49358-549 |
Proprietary Name: | MDSOLARSCIENCES |
Non Proprietary Name: | Avobenzone, Octisalate, and Octocrylene |
Active Ingredient(s): | 30; 50; 27.5 mg/mL; mg/mL; mg/mL & nbsp; Avobenzone, Octisalate, and Octocrylene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49358-549 |
Labeler Name: | MD Solar Sciences |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20130201 |
Package NDC: | 49358-549-01 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (49358-549-01) > 50 mL in 1 BOTTLE, PUMP |
NDC Code | 49358-549-01 |
Proprietary Name | MDSOLARSCIENCES |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (49358-549-01) > 50 mL in 1 BOTTLE, PUMP |
Product NDC | 49358-549 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Octisalate, and Octocrylene |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20130201 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | MD Solar Sciences |
Substance Name | AVOBENZONE; OCTISALATE; OCTOCRYLENE |
Strength Number | 30; 50; 27.5 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |