Package 0031-8771-18

Brand: robitussin honey severe cough, flu plus sore throat

Generic: acetaminophen, dextromethorphan hbr
NDC Package

Package Facts

Identity

Package NDC 0031-8771-18
Digits Only 0031877118
Product NDC 0031-8771
Product ID 0031-8771_35087921-feaf-18e1-e063-6294a90a1471
Description

1 BOTTLE in 1 CARTON (0031-8771-18) / 237 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-06-15
Brand robitussin honey severe cough, flu plus sore throat
Generic acetaminophen, dextromethorphan hbr
Sample Package No

Linked Drug Pages (1)

Robitussin Honey Severe Cough, Flu Plus Sore Throat ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "35087921-feaf-18e1-e063-6294a90a1471", "openfda": {"unii": ["362O9ITL9D", "9D2RTI9KYH"], "rxcui": ["1919076"], "spl_set_id": ["77be57fb-0ae5-4fad-97f3-b6a4b57383a9"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8771-12)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-8771-12", "marketing_start_date": "20200615"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8771-18)  / 237 mL in 1 BOTTLE", "package_ndc": "0031-8771-18", "marketing_start_date": "20200615"}], "brand_name": "Robitussin Honey Severe Cough, Flu Plus Sore Throat", "product_id": "0031-8771_35087921-feaf-18e1-e063-6294a90a1471", "dosage_form": "SOLUTION", "pharm_class": ["Sigma-1 Agonist [EPC]", "Sigma-1 Receptor Agonists [MoA]", "Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC]", "Uncompetitive NMDA Receptor Antagonists [MoA]"], "product_ndc": "0031-8771", "generic_name": "acetaminophen, dextromethorphan hbr", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Honey Severe Cough, Flu Plus Sore Throat", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DEXTROMETHORPHAN HYDROBROMIDE", "strength": "20 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200615", "listing_expiration_date": "20261231"}