Package 58414-0019-1
Brand: neostrata enlighten skin brightener with sunscreen broad spectrum spf 35
Generic: octinoxate, octisalate, and avobenzonePackage Facts
Identity
Package NDC
58414-0019-1
Digits Only
5841400191
Product NDC
58414-0019
Description
1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE
Marketing
Marketing Status
Brand
neostrata enlighten skin brightener with sunscreen broad spectrum spf 35
Generic
octinoxate, octisalate, and avobenzone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2b59538b-e516-a18d-e063-6394a90aeeab", "openfda": {"upc": ["0732013301316"], "unii": ["G63QQF2NOX", "4Y5P7MUD51", "4X49Y0596W"], "spl_set_id": ["ed495f18-2f8e-4991-b797-82e9f6fc7acb"], "manufacturer_name": ["NeoStrata Company Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (58414-0019-1) / 40 g in 1 TUBE", "package_ndc": "58414-0019-1", "marketing_start_date": "20181201"}], "brand_name": "NeoStrata Enlighten Skin Brightener with Sunscreen Broad Spectrum SPF 35", "product_id": "58414-0019_2b59538b-e516-a18d-e063-6394a90aeeab", "dosage_form": "CREAM", "product_ndc": "58414-0019", "generic_name": "Octinoxate, Octisalate, and Avobenzone", "labeler_name": "NeoStrata Company Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "NeoStrata Enlighten Skin Brightener", "brand_name_suffix": "with Sunscreen Broad Spectrum SPF 35", "active_ingredients": [{"name": "AVOBENZONE", "strength": "30 mg/g"}, {"name": "OCTINOXATE", "strength": "75 mg/g"}, {"name": "OCTISALATE", "strength": "50 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20181201", "listing_expiration_date": "20261231"}