Nasal Decongestant

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
Generic name: PSEUDOEPHEDRINE HCL
Manufacturer: Proficient Rx LP
Product type: HUMAN OTC DRUG
SPL set ID: 4eab4344-d95e-4b19-a21e-9c8ad033863a
SPL ID: 076ef551-acae-42de-8948-3e6b0273ebc5
Version: 5
Effective date: 2024-10-01
Source export date: 2026-10-12
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:08:39

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		Nasal Decongestant	openfda.brand_name
generic name		PSEUDOEPHEDRINE HCL	openfda.generic_name
manufacturer name		Proficient Rx LP	openfda.manufacturer_name
ndc	package	63187-344-24	openfda.package_ndc
ndc	product	63187-344	openfda.product_ndc
ndc11	package	63187034424	derived:openfda.package_ndc
rxcui		1049160	openfda.rxcui
spl id		076ef551-acae-42de-8948-3e6b0273ebc5	id
spl set id		4eab4344-d95e-4b19-a21e-9c8ad033863a	set_id
unii		6V9V2RYJ8N	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 2 weeks after stoppin the MAOI drug. If you do not know if your prescription drug contains and MAOI, ask a doctor or pharmacist before taking this product. Ask a doctor before use if you have • diabetes • high blood pressure • heart disease • thyroid disease • 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 • 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 (1-800-222-1222).

Reported adverse events (FAERS/openFDA)#

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