Package 0067-7918-06

Brand: theraflu nighttime severe cold and cough

Generic: acetaminophen, diphenhydramine hcl, phenylephrine hcl
NDC Package

Package Facts

Identity

Package NDC 0067-7918-06
Digits Only 0067791806
Product NDC 0067-7918
Product ID 0067-7918_100acde5-89b2-0bed-e063-6294a90aa1a9
Description

6 PACKET in 1 CARTON (0067-7918-06) / 237 mL in 1 PACKET (0067-7918-01)

Marketing

Marketing Status
Marketed Since 2014-07-01
Brand theraflu nighttime severe cold and cough
Generic acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package No

Linked Drug Pages (2)

Theraflu Multi-Symptom Severe Cold and Theraflu Nighttime Severe Cold and Cough ndc-match (0.95) THERAFLU NIGHTTIME SEVERE COLD AND COUGH ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "100acde5-89b2-0bed-e063-6294a90aa1a9", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1659960"], "spl_set_id": ["5f7f6f70-0f36-4541-89f2-d953259cdb1e"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "6 PACKET in 1 CARTON (0067-7918-06)  / 237 mL in 1 PACKET (0067-7918-01)", "package_ndc": "0067-7918-06", "marketing_start_date": "20140701"}], "brand_name": "THERAFLU NIGHTTIME SEVERE COLD AND COUGH", "product_id": "0067-7918_100acde5-89b2-0bed-e063-6294a90aa1a9", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-7918", "generic_name": "ACETAMINOPHEN, DIPHENHYDRAMINE HCL, PHENYLEPHRINE HCL", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "THERAFLU", "brand_name_suffix": "NIGHTTIME SEVERE COLD AND COUGH", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/237mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/237mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/237mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140701", "listing_expiration_date": "20261231"}