Package 0031-8702-13
Brand: childrens robitussin cough and chest congestion dm
Generic: dextromethorphan hydrobromide and guaifenesinPackage Facts
Identity
Package NDC
0031-8702-13
Digits Only
0031870213
Product NDC
0031-8702
Description
1 BOTTLE in 1 CARTON (0031-8702-13) / 118 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
childrens robitussin cough and chest congestion dm
Generic
dextromethorphan hydrobromide and guaifenesin
Sample Package
No
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6755f338-34be-43e4-9cdf-bf2c2348cbbd", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1790650"], "spl_set_id": ["15950273-14c9-4a0b-bbb4-683048add722"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8702-13) / 118 mL in 1 BOTTLE", "package_ndc": "0031-8702-13", "marketing_start_date": "20200512"}], "brand_name": "Childrens Robitussin Cough and Chest Congestion DM", "product_id": "0031-8702_6755f338-34be-43e4-9cdf-bf2c2348cbbd", "dosage_form": "LIQUID", "pharm_class": ["Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0031-8702", "generic_name": "dextromethorphan hydrobromide and guaifenesin", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Childrens Robitussin Cough and Chest Congestion DM", "active_ingredients": [{"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}, {"name": "GUAIFENESIN", "strength": "200 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200512", "listing_expiration_date": "20261231"}