Package 0363-0460-06

Brand: nighttime cold and flu maximum strength

Generic: acetaminophen, diphenhydramine hci, phenylephrine hci
NDC Package

Package Facts

Identity

Package NDC 0363-0460-06
Digits Only 0363046006
Product NDC 0363-0460
Product ID 0363-0460_67d2f459-957e-49f4-8f75-b82d57b3402a
Description

177 mL in 1 BOTTLE, PLASTIC (0363-0460-06)

Marketing

Marketing Status
Marketed Since 2015-06-30
Brand nighttime cold and flu maximum strength
Generic acetaminophen, diphenhydramine hci, phenylephrine hci
Sample Package No

Linked Drug Pages (2)

Daytime Mucus Relief Severe Congestion and Cough and Nighttime Cold and Flu Maximum Strength ndc-match (0.95) Nighttime Cold and Flu Maximum Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "67d2f459-957e-49f4-8f75-b82d57b3402a", "openfda": {"upc": ["0311917177762"], "unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1375932"], "spl_set_id": ["37896933-3ed3-457f-8a32-ee0d784a19e8"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (0363-0460-06)", "package_ndc": "0363-0460-06", "marketing_start_date": "20150630"}], "brand_name": "Nighttime Cold and Flu Maximum Strength", "product_id": "0363-0460_67d2f459-957e-49f4-8f75-b82d57b3402a", "dosage_form": "LIQUID", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "0363-0460", "generic_name": "Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nighttime Cold and Flu", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "650 mg/20mL"}, {"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "25 mg/20mL"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/20mL"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20150630", "listing_expiration_date": "20261231"}