Package 85053-002-01

Brand: woodsleep tallow sunscreen

Generic: titanium dioxide
NDC Package

Package Facts

Identity

Package NDC 85053-002-01
Digits Only 8505300201
Product NDC 85053-002
Description

57 mg in 1 BOX (85053-002-01)

Marketing

Marketing Status
Marketed Since 2025-04-18
Brand woodsleep tallow sunscreen
Generic titanium dioxide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "448bdbfa-2de6-fce8-e063-6394a90a2cf7", "openfda": {"unii": ["98HPY76U4W"], "spl_set_id": ["330a9f2e-7ce1-f83f-e063-6394a90a184a"], "manufacturer_name": ["Shantou Woodsleep Biotechnology Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "57 mg in 1 BOX (85053-002-01)", "package_ndc": "85053-002-01", "marketing_start_date": "20250418"}], "brand_name": "WOODSLEEP Tallow Sunscreen", "product_id": "85053-002_448bdbfa-2de6-fce8-e063-6394a90a2cf7", "dosage_form": "CREAM", "product_ndc": "85053-002", "generic_name": "TITANIUM DIOXIDE", "labeler_name": "Shantou Woodsleep Biotechnology Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "WOODSLEEP Tallow Sunscreen", "active_ingredients": [{"name": "TALLOW", "strength": ".0114 mg/57mg"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250418", "listing_expiration_date": "20261231"}