Product NDC: | 0299-3930 |
Proprietary Name: | Cetaphil Daily Facial Moisturizer SPF 50 |
Non Proprietary Name: | octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide |
Active Ingredient(s): | 7.5; 5; 7; 6; 5.7 mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL & nbsp; octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LOTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0299-3930 |
Labeler Name: | Galderma Laboratories, L.P. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120101 |
Package NDC: | 0299-3930-02 |
Package Description: | 1 TUBE in 1 CARTON (0299-3930-02) > 50 mL in 1 TUBE |
NDC Code | 0299-3930-02 |
Proprietary Name | Cetaphil Daily Facial Moisturizer SPF 50 |
Package Description | 1 TUBE in 1 CARTON (0299-3930-02) > 50 mL in 1 TUBE |
Product NDC | 0299-3930 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide |
Dosage Form Name | LOTION |
Route Name | TOPICAL |
Start Marketing Date | 20120101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Galderma Laboratories, L.P. |
Substance Name | OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE |
Strength Number | 7.5; 5; 7; 6; 5.7 |
Strength Unit | mL/100mL; mL/100mL; mL/100mL; mL/100mL; mL/100mL |
Pharmaceutical Classes |