Package 0031-0101-04

Brand: robitussin maximum strength severe multi-symptom cough cold flu nighttime

Generic: acetaminophen, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 0031-0101-04
Digits Only 0031010104
Product NDC 0031-0101
Description

1 BOTTLE in 1 CARTON (0031-0101-04) / 118 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-02-15
Brand robitussin maximum strength severe multi-symptom cough cold flu nighttime
Generic acetaminophen, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0f9df094-b106-76fc-e063-6294a90a6a18", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40"], "rxcui": ["2374554"], "spl_set_id": ["721bfee2-0d3d-4d8b-beee-1ea83064d1c8"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0031-0101-04)  / 118 mL in 1 BOTTLE", "package_ndc": "0031-0101-04", "marketing_start_date": "20240215"}], "brand_name": "Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu Nighttime", "product_id": "0031-0101_0f9df094-b106-76fc-e063-6294a90a6a18", "dosage_form": "LIQUID", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "0031-0101", "generic_name": "acetaminophen, diphenhydramine hcl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Robitussin Maximum Strength Severe Multi-Symptom Cough Cold Flu 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": "20240215", "listing_expiration_date": "20261231"}