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Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen - 49967-595-01 - (Titanium dioxide)
Drug Information of Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
| Product NDC: | 49967-595 |
| Proprietary Name: | Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen |
| Non Proprietary Name: | Titanium dioxide |
| Active Ingredient(s): | 110 mg/mL & nbsp; Titanium dioxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
| Product NDC: | 49967-595 |
| Labeler Name: | L'Oreal USA Products Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130601 |
Package Information of Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
| Package NDC: | 49967-595-01 |
| Package Description: | 150 mL in 1 BOTTLE, PLASTIC (49967-595-01) |
NDC Information of Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen
| NDC Code | 49967-595-01 |
| Proprietary Name | Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen |
| Package Description | 150 mL in 1 BOTTLE, PLASTIC (49967-595-01) |
| Product NDC | 49967-595 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Titanium dioxide |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | L'Oreal USA Products Inc |
| Substance Name | TITANIUM DIOXIDE |
| Strength Number | 110 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
