Product NDC: | 63550-851 |
Proprietary Name: | SUN DEFENSE SPF 30 |
Non Proprietary Name: | Avobenzone Octinoxate Oxybenzone Titanium dioxide |
Active Ingredient(s): | 25; 75; 6; 20 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; Avobenzone Octinoxate Oxybenzone Titanium dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63550-851 |
Labeler Name: | Kamins Dermatologics Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110902 |
Package NDC: | 63550-851-10 |
Package Description: | 120 mL in 1 BOX (63550-851-10) |
NDC Code | 63550-851-10 |
Proprietary Name | SUN DEFENSE SPF 30 |
Package Description | 120 mL in 1 BOX (63550-851-10) |
Product NDC | 63550-851 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone Octinoxate Oxybenzone Titanium dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20110902 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kamins Dermatologics Inc. |
Substance Name | AVOBENZONE; OCTINOXATE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 25; 75; 6; 20 |
Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |