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

Labeler: walgreens
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name daytime mucus relief severe cold and nighttime cold and flu maximum strength
Generic Name daytime acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, nighttime acetaminophen, diphenhydramine hci, phenylephrine hci
Labeler walgreens
Dosage Form KIT
Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-0463
Product ID 0363-0463_1ad0ce30-ad63-43bb-bb52-e94cf0eebc6f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2016-03-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03630463
Hyphenated Format 0363-0463

Supplemental Identifiers

RxCUI
1116572 1375932 1424850
UPC
0311917177786

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name daytime mucus relief severe cold and nighttime cold and flu maximum strength (source: ndc)
Generic Name daytime acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hci, nighttime acetaminophen, diphenhydramine hci, phenylephrine hci (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 650 mg
  • 25 mg
  • 10 mg
  • 20 mg
  • 400 mg
source: label
Packaging
  • 1 KIT in 1 KIT (0363-0463-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

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

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

DayTime Mucus Relief Severe Cold and Nighttime Cold and Flu Maximum Strength ndc-match (0.9)

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"}