| Product NDC: | 67692-241 |
| Proprietary Name: | LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen |
| Non Proprietary Name: | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Active Ingredient(s): | 30; 70; 20; 27 mg/mL; mg/mL; mg/mL; mg/mL & nbsp; AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 67692-241 |
| Labeler Name: | LUMENE OY |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121129 |
| Package NDC: | 67692-241-00 |
| Package Description: | 50 mL in 1 BOTTLE (67692-241-00) |
| NDC Code | 67692-241-00 |
| Proprietary Name | LUMENE Sensitive Touch Daily Moisture SPF 15 Sunscreen |
| Package Description | 50 mL in 1 BOTTLE (67692-241-00) |
| Product NDC | 67692-241 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | AVOBENZONE, OCTINOXATE, OCTISALATE, OXYBENZONE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121129 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | LUMENE OY |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OCTOCRYLENE |
| Strength Number | 30; 70; 20; 27 |
| Strength Unit | mg/mL; mg/mL; mg/mL; mg/mL |
| Pharmaceutical Classes |