gnp mucus relief pe

Generic: guaifenesin/phenylephrine

Labeler: amerisourcebergen drug corp
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name gnp mucus relief pe
Generic Name guaifenesin/phenylephrine
Labeler amerisourcebergen drug corp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

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

Manufacturer
AmerisourceBergen Drug Corp

Identifiers & Regulatory

Product NDC 46122-700
Product ID 46122-700_d97803b2-8d2a-42a1-9864-581cf86f698c
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M012
Listing Expiration 2026-12-31
Marketing Start 2022-01-13

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 46122700
Hyphenated Format 46122-700

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 gnp mucus relief pe (source: ndc)
Generic Name guaifenesin/phenylephrine (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 in 1 CARTON (46122-700-71) / 50 TABLET in 1 BOTTLE
source: ndc

Packages (1)

46122-700-71 1 BOTTLE in 1 CARTON (46122-700-71) / 50 TABLET in 1 BOTTLE

Ingredients (2)

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

Linked Drug Pages (1)

GNP Mucus Relief PE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d97803b2-8d2a-42a1-9864-581cf86f698c", "openfda": {"nui": ["N0000193956", "N0000008867", "N0000009560"], "unii": ["495W7451VQ", "04JA59TNSJ"], "rxcui": ["1304111"], "spl_set_id": ["63932e68-b09d-4500-bc1d-cfb2c267df1c"], "pharm_class_pe": ["Decreased Respiratory Secretion Viscosity [PE]", "Increased Respiratory Secretions [PE]"], "pharm_class_epc": ["Expectorant [EPC]"], "manufacturer_name": ["AmerisourceBergen Drug Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (46122-700-71)  / 50 TABLET in 1 BOTTLE", "package_ndc": "46122-700-71", "marketing_start_date": "20220113"}], "brand_name": "GNP Mucus Relief PE", "product_id": "46122-700_d97803b2-8d2a-42a1-9864-581cf86f698c", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha1-Agonists [MoA]", "Decreased Respiratory Secretion Viscosity [PE]", "Expectorant [EPC]", "Increased Respiratory Secretions [PE]", "alpha-1 Adrenergic Agonist [EPC]"], "product_ndc": "46122-700", "generic_name": "Guaifenesin/phenylephrine", "labeler_name": "AmerisourceBergen Drug Corp", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GNP Mucus Relief", "brand_name_suffix": "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": "20220113", "listing_expiration_date": "20261231"}