Package 0031-8770-12

Brand: robitussin honey severe cough, flu plus sore throat nighttime

Generic: acetaminophen and diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0031-8770-12
Digits Only 0031877012
Product NDC 0031-8770
Product ID 0031-8770_e1aff09c-8c75-45af-b83c-71be0cb7309b
Description

1 BOTTLE in 1 CARTON (0031-8770-12) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2020-06-15
Brand robitussin honey severe cough, flu plus sore throat nighttime
Generic acetaminophen and diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

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

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e1aff09c-8c75-45af-b83c-71be0cb7309b", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["2374554"], "spl_set_id": ["7decc168-e847-4bbe-910b-26081469406f"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8770-12)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-8770-12", "marketing_start_date": "20200615"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-8770-18)  / 237 mL in 1 BOTTLE", "package_ndc": "0031-8770-18", "marketing_start_date": "20200615"}], "brand_name": "Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime", "product_id": "0031-8770_e1aff09c-8c75-45af-b83c-71be0cb7309b", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0031-8770", "generic_name": "acetaminophen and diphenhydramine hydrochloride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttime", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200615", "listing_expiration_date": "20261231"}