Package 72036-167-02

Brand: mucus relief sinus severe congestion and pain

Generic: acetaminophen, guaifenesin, and phenylephrine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72036-167-02
Digits Only 7203616702
Product NDC 72036-167
Description

2 BLISTER PACK in 1 CARTON (72036-167-02) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-02-04
Brand mucus relief sinus severe congestion and pain
Generic acetaminophen, guaifenesin, and phenylephrine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "25157fb6-a5a4-e140-e063-6394a90a73cc", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["362O9ITL9D", "495W7451VQ", "04JA59TNSJ"], "rxcui": ["1243679"], "spl_set_id": ["b96c376e-578f-1124-e053-2a95a90acbb4"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["HARRIS TEETER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (72036-167-02)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "72036-167-02", "marketing_start_date": "20210204"}], "brand_name": "Mucus Relief Sinus Severe Congestion and Pain", "product_id": "72036-167_25157fb6-a5a4-e140-e063-6394a90a73cc", "dosage_form": "TABLET, COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "72036-167", "generic_name": "ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE", "labeler_name": "HARRIS TEETER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief Sinus Severe Congestion and Pain", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "GUAIFENESIN", "strength": "200 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210204", "listing_expiration_date": "20261231"}