Package 0067-8137-20
Brand: theraflu expressmax nighttime severe cold and cough
Generic: acetaminophen, diphenhydramine hcl, phenylephrine hclPackage Facts
Identity
Package NDC
0067-8137-20
Digits Only
0067813720
Product NDC
0067-8137
Description
2 BLISTER PACK in 1 CARTON (0067-8137-20) / 10 TABLET, FILM COATED in 1 BLISTER PACK
Marketing
Marketing Status
Brand
theraflu expressmax nighttime severe cold and cough
Generic
acetaminophen, diphenhydramine hcl, phenylephrine hcl
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "13185fea-1e12-cf5a-e063-6394a90a18af", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1233575"], "spl_set_id": ["62f7fcb9-e31a-4634-b1c2-44a9567e3a61"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (0067-8137-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0067-8137-10", "marketing_start_date": "20170608"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (0067-8137-20) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0067-8137-20", "marketing_start_date": "20160705"}], "brand_name": "Theraflu ExpressMax Nighttime Severe Cold and Cough", "product_id": "0067-8137_13185fea-1e12-cf5a-e063-6394a90a18af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0067-8137", "generic_name": "acetaminophen, diphenhydramine HCl, phenylephrine HCl", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Theraflu ExpressMax", "brand_name_suffix": "Nighttime Severe Cold and Cough", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "12.5 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160705", "listing_expiration_date": "20261231"}