Nasal Decongestant PE Maximum Strength Non-Drowsy

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Nasal Decongestant PE Maximum Strength Non-Drowsy
Generic name: PHENYLEPHRINE 10 MG
Manufacturer: Allegiant Health
Product type: HUMAN OTC DRUG
SPL set ID: 7aef00df-816a-4ea2-a2ad-beed66dd2fe4
SPL ID: d6f9b26d-57c2-492c-aafd-baf2f1ffd3e3
Version: 10
Effective date: 2018-11-07
Source export date: 2026-10-12
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:38:23

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Nasal Decongestant PE Maximum Strength Non-Drowsy	openfda.brand_name
generic name		PHENYLEPHRINE 10 MG	openfda.generic_name
manufacturer name		Allegiant Health	openfda.manufacturer_name
ndc	package	69168-272-93	openfda.package_ndc
ndc	package	69168-272-17	openfda.package_ndc
ndc	package	69168-272-82	openfda.package_ndc
ndc	product	69168-272	openfda.product_ndc
ndc11	package	69168027217	derived:openfda.package_ndc
ndc11	package	69168027293	derived:openfda.package_ndc
ndc11	package	69168027282	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		d6f9b26d-57c2-492c-aafd-baf2f1ffd3e3	id
spl set id		7aef00df-816a-4ea2-a2ad-beed66dd2fe4	set_id
unii		04JA59TNSJ	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use Do not use if you are now taking a prescription mono-amine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have heart disease high blood pressure thyroid disease diabetes trouble urinating due to an enlarged prostate gland When using this product do not use more than directed Stop use and ask a doctor if you get nervous, dizzy, or sleepless symptoms do not improve within 7 days or are accompanied by fever

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.