Package 0031-8715-10

Brand: childrens robitussin cough and chest congestion dm

Generic: dextromethorphan hydrobromide, guaifenesin
NDC Package

Package Facts

Identity

Package NDC 0031-8715-10
Digits Only 0031871510
Product NDC 0031-8715
Description

1 BOTTLE in 1 CARTON (0031-8715-10) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2014-07-01
Brand childrens robitussin cough and chest congestion dm
Generic dextromethorphan hydrobromide, guaifenesin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13dd51f2-2aca-082e-e063-6294a90a2f4f", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["9D2RTI9KYH", "495W7451VQ"], "rxcui": ["1020138"], "spl_set_id": ["b9772292-9eb6-47cf-abb8-007c25478090"], "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 (0031-8715-10)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-8715-10", "marketing_start_date": "20140701"}], "brand_name": "Childrens Robitussin Cough and Chest Congestion DM", "product_id": "0031-8715_13dd51f2-2aca-082e-e063-6294a90a2f4f", "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": "0031-8715", "generic_name": "dextromethorphan hydrobromide, 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": "5 mg/5mL"}, {"name": "GUAIFENESIN", "strength": "100 mg/5mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}