Package 83447-005-01

Brand: renewaluxe spf 50 sunscreen

Generic: renewaluxe spf 50 sunscreen
NDC Package

Package Facts

Identity

Package NDC 83447-005-01
Digits Only 8344700501
Product NDC 83447-005
Description

50 mL in 1 BOX (83447-005-01)

Marketing

Marketing Status
Marketed Since 2024-06-26
Brand renewaluxe spf 50 sunscreen
Generic renewaluxe spf 50 sunscreen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["CUTANEOUS"], "spl_id": "47b31ef5-e027-ed4b-e063-6294a90a2d30", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["1bc29960-5e73-e8ab-e063-6294a90a3f80"], "manufacturer_name": ["Guangzhou Fantesy Biotechnology Co.,Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOX (83447-005-01)", "package_ndc": "83447-005-01", "marketing_start_date": "20240626"}], "brand_name": "RENEWALUXE SPF 50 Sunscreen", "product_id": "83447-005_47b31ef5-e027-ed4b-e063-6294a90a2d30", "dosage_form": "CREAM", "product_ndc": "83447-005", "generic_name": "RENEWALUXE SPF 50 Sunscreen", "labeler_name": "Guangzhou Fantesy Biotechnology Co.,Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "RENEWALUXE SPF 50 Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "21.8 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240626", "listing_expiration_date": "20271231"}