Package 49967-203-02

{"route": ["TOPICAL"], "spl_id": "ff588e86-0a43-4b6f-a916-5018e807d227", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["83725be5-4a0a-4717-a034-ff2999dd4099"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (49967-203-01)  / 50 mL in 1 BOTTLE", "package_ndc": "49967-203-01", "marketing_start_date": "20231215"}, {"sample": false, "description": "1 TUBE in 1 CARTON (49967-203-02)  / 5 mL in 1 TUBE", "package_ndc": "49967-203-02", "marketing_start_date": "20231215"}], "brand_name": "La Roche Posay Laboratoire Dermatologique Anthelios Tinted Mineral Light Fluid Sunscreen Broad Spectrum SPF 40 Deep", "product_id": "49967-203_ff588e86-0a43-4b6f-a916-5018e807d227", "dosage_form": "LOTION", "product_ndc": "49967-203", "generic_name": "Titanium dioxide and Zinc oxide", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "La Roche Posay Laboratoire Dermatologique Anthelios Tinted Mineral Light Fluid Sunscreen Broad Spectrum SPF 40 Deep", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "170 mg/mL"}, {"name": "ZINC OXIDE", "strength": "80 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231215", "listing_expiration_date": "20261231"}