| Product NDC: | 49527-028 |
| Proprietary Name: | MOISTURE SURGE CC |
| Non Proprietary Name: | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Active Ingredient(s): | .08175; .0555; .5772; .0355 g/mL; g/mL; g/mL; g/mL & nbsp; OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49527-028 |
| Labeler Name: | CLINIQUE LABORATORIES INC. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130101 |
| Package NDC: | 49527-028-01 |
| Package Description: | 1 BOTTLE in 1 CARTON (49527-028-01) > 40 mL in 1 BOTTLE |
| NDC Code | 49527-028-01 |
| Proprietary Name | MOISTURE SURGE CC |
| Package Description | 1 BOTTLE in 1 CARTON (49527-028-01) > 40 mL in 1 BOTTLE |
| Product NDC | 49527-028 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE, and ZINC OXIDE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | CLINIQUE LABORATORIES INC. |
| Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
| Strength Number | .08175; .0555; .5772; .0355 |
| Strength Unit | g/mL; g/mL; g/mL; g/mL |
| Pharmaceutical Classes |