mucus relief all in one maximum strength

Generic: 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 maximum strength
Generic Name acetaminophen, diphenhydramine hcl phenylephrine hcl
Labeler walgreens
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

acetaminophen 650 mg/20mL, diphenhydramine hydrochloride 25 mg/20mL, phenylephrine hydrochloride 10 mg/20mL

Manufacturer
Walgreens

Identifiers & Regulatory

Product NDC 0363-9130
Product ID 0363-9130_77bb2566-dd92-4d40-8841-dd7d7c609499
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2021-08-27

Pharmacologic Class

Classes
adrenergic alpha1-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-1 adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03639130
Hyphenated Format 0363-9130

Supplemental Identifiers

RxCUI
1375932
UNII
362O9ITL9D TC2D6JAD40 04JA59TNSJ

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 maximum strength (source: ndc)
Generic Name acetaminophen, diphenhydramine hcl phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 650 mg/20mL
  • 25 mg/20mL
  • 10 mg/20mL
source: ndc
Packaging
  • 177 mL in 1 BOTTLE, PLASTIC (0363-9130-06)
source: ndc

Packages (1)

0363-9130-06 177 mL in 1 BOTTLE, PLASTIC (0363-9130-06)

Ingredients (3)

acetaminophen (650 mg/20mL) diphenhydramine hydrochloride (25 mg/20mL) phenylephrine hydrochloride (10 mg/20mL)

Linked Drug Pages (1)

Mucus Relief All in One Maximum Strength ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "77bb2566-dd92-4d40-8841-dd7d7c609499", "openfda": {"unii": ["362O9ITL9D", "TC2D6JAD40", "04JA59TNSJ"], "rxcui": ["1375932"], "spl_set_id": ["a33ae35b-1cde-4a3d-a836-3b169e4f1bb9"], "manufacturer_name": ["Walgreens"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 BOTTLE, PLASTIC (0363-9130-06)", "package_ndc": "0363-9130-06", "marketing_start_date": "20210827"}], "brand_name": "Mucus Relief All in One Maximum Strength", "product_id": "0363-9130_77bb2566-dd92-4d40-8841-dd7d7c609499", "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": "0363-9130", "generic_name": "Acetaminophen, Diphenhydramine HCl Phenylephrine HCl", "labeler_name": "Walgreens", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief All in One", "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": "20210827", "listing_expiration_date": "20261231"}