Package 49967-595-01

Brand: kiehls since 1851 activated sun protector for face and body broad spectrum spf 50 sunscreen

Generic: titanium dioxide
NDC Package

Package Facts

Identity

Package NDC 49967-595-01
Digits Only 4996759501
Product NDC 49967-595
Product ID 49967-595_676f1412-f75f-4dc4-a76a-57c360aeb54c
Description

150 mL in 1 BOTTLE, PLASTIC (49967-595-01)

Marketing

Marketing Status
Marketed Since 2013-06-01
Brand kiehls since 1851 activated sun protector for face and body broad spectrum spf 50 sunscreen
Generic titanium dioxide
Sample Package No

Linked Drug Pages (1)

Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "676f1412-f75f-4dc4-a76a-57c360aeb54c", "openfda": {"upc": ["3605970205959"], "unii": ["15FIX9V2JP"], "spl_set_id": ["87496037-36ca-4c5f-973f-46626cf4096e"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 mL in 1 BOTTLE, PLASTIC (49967-595-01)", "package_ndc": "49967-595-01", "marketing_start_date": "20130601"}], "brand_name": "Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen", "product_id": "49967-595_676f1412-f75f-4dc4-a76a-57c360aeb54c", "dosage_form": "LOTION", "product_ndc": "49967-595", "generic_name": "Titanium dioxide", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kiehls Since 1851 Activated Sun Protector For Face and Body Broad Spectrum SPF 50 Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "110 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130601", "listing_expiration_date": "20261231"}