Package 49404-153-01

{"route": ["TOPICAL"], "spl_id": "47ed472b-224a-5b9a-e063-6394a90a7030", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["f06c31b4-da5f-6495-e053-2995a90ae67c"], "manufacturer_name": ["Have & Be Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (49404-153-01)  / 50 mL in 1 TUBE", "package_ndc": "49404-153-01", "marketing_start_date": "20221222"}, {"sample": false, "description": "5 mL in 1 TUBE (49404-153-02)", "package_ndc": "49404-153-02", "marketing_start_date": "20221222"}], "brand_name": "DR.JART EVERY SUN DAY MINERAL SUN SCREEN", "product_id": "49404-153_47ed472b-224a-5b9a-e063-6394a90a7030", "dosage_form": "CREAM", "product_ndc": "49404-153", "generic_name": "Titanium dioxide, Zinc Oxide", "labeler_name": "Have & Be Co., Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DR.JART EVERY SUN DAY MINERAL SUN SCREEN", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "41 mg/mL"}, {"name": "ZINC OXIDE", "strength": "115 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221222", "listing_expiration_date": "20271231"}