Package 42829-401-01

{"route": ["NASAL"], "spl_id": "2d073cca-7bcc-d1bd-e063-6294a90a0c39", "openfda": {"unii": ["8MDF5V39QO", "451W47IQ8X"], "rxcui": ["1542919"], "spl_set_id": ["c33bf872-54aa-45e0-9e40-a6565a13f198"], "manufacturer_name": ["ASCENT CONSUMER PRODUCTS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3000 mg in 1 PACKET (42829-401-01)", "package_ndc": "42829-401-01", "marketing_start_date": "20150201"}], "brand_name": "SinuCleanse", "product_id": "42829-401_2d073cca-7bcc-d1bd-e063-6294a90a0c39", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Osmotic Laxative [EPC]"], "product_ndc": "42829-401", "generic_name": "SODIUM BICARBONATE, SODIUM CHLORIDE", "labeler_name": "ASCENT CONSUMER PRODUCTS, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SinuCleanse", "active_ingredients": [{"name": "SODIUM BICARBONATE", "strength": "700 mg/3000mg"}, {"name": "SODIUM CHLORIDE", "strength": "2300 mg/3000mg"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20150201", "listing_expiration_date": "20261231"}