| 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 |