Nasal Decongestant PE Non-Drowsy Maximum Strength

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 Non-Drowsy Maximum Strength
Generic name: PHENYLEPHRINE HCL
Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC
Product type: HUMAN OTC DRUG
SPL set ID: bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d
SPL ID: d534021e-9167-4966-bd79-d13ee792282b
Version: 18
Effective date: 2026-01-12
Source export date: 2026-10-12
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/a497e765d824a2e2aa9e88d5f0eea2aae9dcba363989e5f163395cda5c3c9dd8/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:46:00

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 Non-Drowsy Maximum Strength	openfda.brand_name
generic name		PHENYLEPHRINE HCL	openfda.generic_name
manufacturer name		CHAIN DRUG MARKETING ASSOCIATION INC	openfda.manufacturer_name
ndc	package	63868-144-74	openfda.package_ndc
ndc	package	63868-144-37	openfda.package_ndc
ndc	package	63868-144-19	openfda.package_ndc
ndc	product	63868-144	openfda.product_ndc
ndc11	package	63868014437	derived:openfda.package_ndc
ndc11	package	63868014474	derived:openfda.package_ndc
ndc11	package	63868014419	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		d534021e-9167-4966-bd79-d13ee792282b	id
spl set id		bf7246c1-90fe-4de8-8bb2-e5ff7e8ca63d	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 if you are now taking a prescription monoamine 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 diabetes thyroid disease high blood pressure difficulty in urination due to enlargement of the prostate gland When using this product do not exceed recommended dosage. Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur symptoms do not improve within 7 days or occur with fever If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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