mucus relief pe sinus congestion

Generic: guaifenesin, phenylephrine hcl

Labeler: cardinal health 110, llc. dba leader
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief pe sinus congestion
Generic Name guaifenesin, phenylephrine hcl
Labeler cardinal health 110, llc. dba leader
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

guaifenesin 400 mg/1, phenylephrine hydrochloride 10 mg/1

Manufacturer
Cardinal Health 110, LLC. DBA Leader

Identifiers & Regulatory

Product NDC 70000-0141
Product ID 70000-0141_59fa21ab-5e68-467b-90bf-2c8a3e96709b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2006-04-15

Pharmacologic Class

Established (EPC)
expectorant [epc]
Physiologic Effect
decreased respiratory secretion viscosity [pe] increased respiratory secretions [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 700000141
Hyphenated Format 70000-0141

Supplemental Identifiers

RxCUI
1304111
UPC
0096295143584
UNII
495W7451VQ 04JA59TNSJ
NUI
N0000193956 N0000008867 N0000009560

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 pe sinus congestion (source: ndc)
Generic Name guaifenesin, phenylephrine hcl (source: ndc)
Application Number M012 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 400 mg/1
  • 10 mg/1
source: ndc
Packaging
  • 1 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

70000-0141-1 1 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Ingredients (2)

guaifenesin (400 mg/1) phenylephrine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Mucus Relief PE Sinus Congestion ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "59fa21ab-5e68-467b-90bf-2c8a3e96709b", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "upc": ["0096295143584"], "unii": ["495W7451VQ", "04JA59TNSJ"], "rxcui": ["1304111"], "spl_set_id": ["b9129c7b-c869-436f-ab95-269610ef2d9f"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Cardinal Health 110, LLC. DBA Leader"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (70000-0141-1)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "70000-0141-1", "marketing_start_date": "20060415"}], "brand_name": "Mucus Relief PE Sinus Congestion", "product_id": "70000-0141_59fa21ab-5e68-467b-90bf-2c8a3e96709b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "70000-0141", "generic_name": "Guaifenesin, Phenylephrine HCl", "labeler_name": "Cardinal Health 110, LLC. DBA Leader", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief PE Sinus Congestion", "active_ingredients": [{"name": "GUAIFENESIN", "strength": "400 mg/1"}, {"name": "PHENYLEPHRINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "M012", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20060415", "listing_expiration_date": "20261231"}