Package 52358-0004-2

Brand: sunblocz

Generic: zinc oxide
NDC Package

Package Facts

Identity

Package NDC 52358-0004-2
Digits Only 5235800042
Product NDC 52358-0004
Product ID 52358-0004_259f1fe0-327b-a04f-e063-6394a90a534d
Description

118 mL in 1 TUBE (52358-0004-2)

Marketing

Marketing Status
Marketed Since 2018-06-07
Brand sunblocz
Generic zinc oxide
Sample Package No

Linked Drug Pages (1)

Sunblocz ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "259f1fe0-327b-a04f-e063-6394a90a534d", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["36fec1f1-5e8b-5764-e054-00144ff8d46c"], "manufacturer_name": ["Olen Skin Care Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "118 mL in 1 TUBE (52358-0004-2)", "package_ndc": "52358-0004-2", "marketing_start_date": "20180607"}], "brand_name": "Sunblocz", "product_id": "52358-0004_259f1fe0-327b-a04f-e063-6394a90a534d", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "52358-0004", "generic_name": "Zinc oxide", "labeler_name": "Olen Skin Care Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sunblocz", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "43.4 g/177mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160621", "listing_expiration_date": "20261231"}