Package 0067-7919-12

Brand: theraflu multi-symptom severe cold and theraflu nighttime severe cold and cough

Generic: acetaminophen, dextromethorphan hbr, phenylephrine hcl, diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-7919-12
Digits Only 0067791912
Product NDC 0067-7919
Product ID 0067-7919_15bf1214-572a-f6b6-e063-6394a90ab0cb
Description

1 KIT in 1 PACKAGE, COMBINATION (0067-7919-12) * 6 PACKET in 1 CARTON (0067-6426-06) / 237 mL in 1 PACKET (0067-6426-01) * 6 PACKET in 1 CARTON (0067-7918-06) / 237 mL in 1 PACKET (0067-7918-01)

Marketing

Marketing Status
Marketed Since 2016-01-01
Brand theraflu multi-symptom severe cold and theraflu nighttime severe cold and cough
Generic acetaminophen, dextromethorphan hbr, phenylephrine hcl, diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Theraflu Multi-Symptom Severe Cold and Theraflu Nighttime Severe Cold and Cough ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "15bf1214-572a-f6b6-e063-6394a90ab0cb", "openfda": {"rxcui": ["1189316", "1659960", "2640034"], "spl_set_id": ["b06b64c5-dbb4-4ef5-af18-3d7d4979c02f"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 PACKAGE, COMBINATION (0067-7919-12)  *  6 PACKET in 1 CARTON (0067-6426-06)  / 237 mL in 1 PACKET (0067-6426-01)  *  6 PACKET in 1 CARTON (0067-7918-06)  / 237 mL in 1 PACKET (0067-7918-01)", "package_ndc": "0067-7919-12", "marketing_start_date": "20160101"}], "brand_name": "Theraflu Multi-Symptom Severe Cold and Theraflu Nighttime Severe Cold and Cough", "product_id": "0067-7919_15bf1214-572a-f6b6-e063-6394a90ab0cb", "dosage_form": "KIT", "product_ndc": "0067-7919", "generic_name": "Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl, Diphenhydramine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu Multi-Symptom Severe Cold and Theraflu Nighttime Severe Cold and Cough", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160101", "listing_expiration_date": "20261231"}