Package 0363-0463-12

Brand: daytime mucus relief severe cold and nighttime cold and flu maximum strength

Generic: daytime acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, nighttime acetaminophen, diphenhydramine hci, phenylephrine hci
NDC Package

Package Facts

Identity

Package NDC 0363-0463-12
Digits Only 0363046312
Product NDC 0363-0463
Product ID 0363-0463_1ad0ce30-ad63-43bb-bb52-e94cf0eebc6f
Description

1 KIT in 1 KIT (0363-0463-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Marketed Since 2016-03-31
Brand daytime mucus relief severe cold and nighttime cold and flu maximum strength
Generic daytime acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, nighttime acetaminophen, diphenhydramine hci, phenylephrine hci
Sample Package No

Linked Drug Pages (1)

DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "1ad0ce30-ad63-43bb-bb52-e94cf0eebc6f", "openfda": {"upc": ["0311917177786"], "rxcui": ["1116572", "1375932", "1424850"], "spl_set_id": ["3b4b3b04-eff9-4e06-8b37-f6729671d07f"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (0363-0463-12)  *  177 mL in 1 BOTTLE, PLASTIC *  177 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0463-12", "marketing_start_date": "20160331"}], "brand_name": "DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength", "product_id": "0363-0463_1ad0ce30-ad63-43bb-bb52-e94cf0eebc6f", "dosage_form": "KIT", "product_ndc": "0363-0463", "generic_name": "Daytime Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, NightTime Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20160331", "listing_expiration_date": "20261231"}