Package 71220-087-08

{"route": ["TOPICAL"], "spl_id": "2619fd9d-f9e1-18c1-e063-6394a90aa334", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["0e9cd3e5-cff8-7594-e063-6394a90aad90"], "manufacturer_name": ["Innisfree Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (71220-087-08)  / 50 mL in 1 TUBE", "package_ndc": "71220-087-08", "marketing_start_date": "20240201"}, {"sample": false, "description": "1 TUBE in 1 BOX (71220-087-41)  / 10 mL in 1 TUBE", "package_ndc": "71220-087-41", "marketing_start_date": "20240701"}], "brand_name": "Innisfree Daily UV Defense Mineral Sunscreen", "product_id": "71220-087_2619fd9d-f9e1-18c1-e063-6394a90aa334", "dosage_form": "LOTION", "product_ndc": "71220-087", "generic_name": "Zinc Oxide Lotion", "labeler_name": "Innisfree Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Innisfree Daily UV Defense Mineral Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "8 g/50mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240201", "listing_expiration_date": "20261231"}