Package 59958-201-01

Brand: dermaroller anhydrous sunscreen spf 30

Generic: titanium dioxide, zinc oxide
NDC Package

Package Facts

Identity

Package NDC 59958-201-01
Digits Only 5995820101
Product NDC 59958-201
Product ID 59958-201_2b5d6b44-2357-bf46-e063-6294a90a378f
Description

30 g in 1 TUBE (59958-201-01)

Marketing

Marketing Status
Marketed Since 2011-03-01
Brand dermaroller anhydrous sunscreen spf 30
Generic titanium dioxide, zinc oxide
Sample Package No

Linked Drug Pages (1)

Dermaroller Anhydrous Sunscreen SPF 30 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2b5d6b44-2357-bf46-e063-6294a90a378f", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["04e82f1b-c893-4795-b7a9-0523e3ec7552"], "manufacturer_name": ["Owen Biosciences, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (59958-201-01)", "package_ndc": "59958-201-01", "marketing_start_date": "20110301"}], "brand_name": "Dermaroller Anhydrous Sunscreen SPF 30", "product_id": "59958-201_2b5d6b44-2357-bf46-e063-6294a90a378f", "dosage_form": "CREAM", "product_ndc": "59958-201", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "Owen Biosciences, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dermaroller Anhydrous Sunscreen", "brand_name_suffix": "SPF 30", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "10.2 g/100g"}, {"name": "ZINC OXIDE", "strength": "3.7 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20110301", "listing_expiration_date": "20261231"}