Product NDC: | 63550-191 |
Proprietary Name: | Matte Moisturizer SPF 15 |
Non Proprietary Name: | OCTINOXATE OCTISALATE AVOBENZONE |
Active Ingredient(s): | 25; 75; 40 mg/mL; mg/mL; mg/mL & nbsp; OCTINOXATE OCTISALATE AVOBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63550-191 |
Labeler Name: | Kamins Dermatologics Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20101018 |
Package NDC: | 63550-191-03 |
Package Description: | 50 mL in 1 BOX (63550-191-03) |
NDC Code | 63550-191-03 |
Proprietary Name | Matte Moisturizer SPF 15 |
Package Description | 50 mL in 1 BOX (63550-191-03) |
Product NDC | 63550-191 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE OCTISALATE AVOBENZONE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20101018 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kamins Dermatologics Inc. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE |
Strength Number | 25; 75; 40 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |