Package 83447-001-01

Brand: sunscreen powder

Generic: sunscreen powder
NDC Package

Package Facts

Identity

Package NDC 83447-001-01
Digits Only 8344700101
Product NDC 83447-001
Description

3.5 g in 1 BOX (83447-001-01)

Marketing

Marketing Status
Marketed Since 2023-05-05
Brand sunscreen powder
Generic sunscreen powder
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["CUTANEOUS"], "spl_id": "479edb42-9157-566b-e063-6394a90a9101", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["fae8ecaf-7a9c-902b-e053-6394a90a5f31"], "manufacturer_name": ["Guangzhou Fantesy Biotechnology Co.,Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3.5 g in 1 BOX (83447-001-01)", "package_ndc": "83447-001-01", "marketing_start_date": "20230505"}], "brand_name": "sunscreen powder", "product_id": "83447-001_479edb42-9157-566b-e063-6394a90a9101", "dosage_form": "POWDER", "product_ndc": "83447-001", "generic_name": "sunscreen powder", "labeler_name": "Guangzhou Fantesy Biotechnology Co.,Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "sunscreen powder", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "25 g/100g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230505", "listing_expiration_date": "20271231"}