mucus relief pe

Generic: guaifenesin, phenylephrine hcl

Labeler: walgreen company
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name mucus relief pe
Generic Name guaifenesin, phenylephrine hcl
Labeler walgreen company
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

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

Manufacturer
Walgreen Company

Identifiers & Regulatory

Product NDC 0363-0542
Product ID 0363-0542_4e877f05-17b9-4b04-a7e6-50b88500c6e3
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 03630542
Hyphenated Format 0363-0542

Supplemental Identifiers

RxCUI
1304111
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 (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 (0363-0542-01) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
source: ndc

Packages (1)

0363-0542-01 1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01) / 30 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 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4e877f05-17b9-4b04-a7e6-50b88500c6e3", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "04JA59TNSJ"], "rxcui": ["1304111"], "spl_set_id": ["cb1c1922-5dc6-520d-e77e-e951726d9701"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (0363-0542-01)  / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "0363-0542-01", "marketing_start_date": "20060415"}], "brand_name": "Mucus Relief PE", "product_id": "0363-0542_4e877f05-17b9-4b04-a7e6-50b88500c6e3", "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": "0363-0542", "generic_name": "Guaifenesin, Phenylephrine HCl", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Mucus Relief PE", "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"}