Package 59062-1000-8

Brand: spf 50 plus sunscreen

Generic: titanium dioxide, octisalate, and zinc oxide
NDC Package

Package Facts

Identity

Package NDC 59062-1000-8
Digits Only 5906210008
Product NDC 59062-1000
Description

236 mL in 1 TUBE (59062-1000-8)

Marketing

Marketing Status
Discontinued 2026-12-31
Brand spf 50 plus sunscreen
Generic titanium dioxide, octisalate, and zinc oxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "a7636b53-d9d4-4c4f-929a-515a8cc78659", "openfda": {"unii": ["4X49Y0596W", "15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["5a4c71fc-aa6f-47f7-8d1d-2af2e726cf9b"], "manufacturer_name": ["KAS Direct LLC dba BabyGanics"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "236 mL in 1 TUBE (59062-1000-8)", "package_ndc": "59062-1000-8", "marketing_end_date": "20261231", "marketing_start_date": "20170724"}], "brand_name": "SPF 50 plus Sunscreen", "product_id": "59062-1000_a7636b53-d9d4-4c4f-929a-515a8cc78659", "dosage_form": "LOTION", "product_ndc": "59062-1000", "generic_name": "Titanium Dioxide, OCTISALATE, and ZINC OXIDE", "labeler_name": "KAS Direct LLC dba BabyGanics", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SPF 50 plus Sunscreen", "active_ingredients": [{"name": "OCTISALATE", "strength": "50 mg/mL"}, {"name": "TITANIUM DIOXIDE", "strength": "30 mg/mL"}, {"name": "ZINC OXIDE", "strength": "60 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20170724"}