mucus relief all in one daytime nighttime cold flu maximum strength

Generic: acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, diphenhydramine hcl phenylephrine hcl

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

Drug Facts

Product Profile

Brand Name mucus relief all in one daytime nighttime cold flu maximum strength
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, diphenhydramine hcl phenylephrine hcl
Labeler walgreens
Dosage Form KIT
Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-9140
Product ID 0363-9140_cc920fba-fe1e-4ca7-aafa-9b91a616581f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2019-09-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03639140
Hyphenated Format 0363-9140

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 mucus relief all in one daytime nighttime cold flu maximum strength (source: ndc)
Generic Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl, acetaminophen, diphenhydramine hcl phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)

Resolved Composition

Strengths
  • 20 ml
  • 650 mg
  • 20 mg
  • 400 mg
  • 10 mg
  • 25 mg
source: label
Packaging
  • 1 KIT in 1 KIT (0363-9140-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

0363-9140-12 1 KIT in 1 KIT (0363-9140-12) * 177 mL in 1 BOTTLE, PLASTIC * 177 mL in 1 BOTTLE, PLASTIC

Ingredients (0)

No ingredient records.

Linked Drug Pages (1)

Mucus Relief All In One Daytime Nighttime Cold Flu Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"spl_id": "cc920fba-fe1e-4ca7-aafa-9b91a616581f", "openfda": {"upc": ["0311917177786"], "rxcui": ["1116572", "1375932", "1424850"], "spl_set_id": ["0b9a4438-7d13-484c-a614-2dedc24974dc"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 KIT in 1 KIT (0363-9140-12)  *  177 mL in 1 BOTTLE, PLASTIC *  177 mL in 1 BOTTLE, PLASTIC", "package_ndc": "0363-9140-12", "marketing_start_date": "20190930"}], "brand_name": "Mucus Relief All In One Daytime Nighttime Cold Flu Maximum Strength", "product_id": "0363-9140_cc920fba-fe1e-4ca7-aafa-9b91a616581f", "dosage_form": "KIT", "product_ndc": "0363-9140", "generic_name": "Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL, Acetaminophen, Diphenhydramine HCL Phenylephrine HCL", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief All In One Daytime Nighttime Cold Flu", "brand_name_suffix": "Maximum Strength", "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190930", "listing_expiration_date": "20261231"}