| 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 |