Product NDC: | 49527-953 |
Proprietary Name: | CLINIQUE CX |
Non Proprietary Name: | OCTINOXATE, OCTISALATE, ZINC OXIDE,TITANIUM DIOXIDE |
Active Ingredient(s): | 7.5; 5; 1.7; 4.6 mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; OCTINOXATE, OCTISALATE, ZINC OXIDE,TITANIUM DIOXIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49527-953 |
Labeler Name: | CLINIQUE LABORATORIES INC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20050501 |
Package NDC: | 49527-953-01 |
Package Description: | 1 TUBE in 1 CARTON (49527-953-01) > 50 mL in 1 TUBE (49527-953-02) |
NDC Code | 49527-953-01 |
Proprietary Name | CLINIQUE CX |
Package Description | 1 TUBE in 1 CARTON (49527-953-01) > 50 mL in 1 TUBE (49527-953-02) |
Product NDC | 49527-953 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OCTISALATE, ZINC OXIDE,TITANIUM DIOXIDE |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20050501 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | CLINIQUE LABORATORIES INC |
Substance Name | OCTINOXATE; OCTISALATE; TITANIUM DIOXIDE; ZINC OXIDE |
Strength Number | 7.5; 5; 1.7; 4.6 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |