NASAL and SINUS 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 and SINUS DECONGESTANT
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: JHK Inc dba American Safety & First Aid
Product type: HUMAN OTC DRUG
SPL set ID: 63e51305-2575-49c4-9fda-7b3e1b4b6ede
SPL ID: 050efff2-4886-4c50-a92c-3f216d200e8a
Version: 2
Effective date: 2024-04-26
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:52:57

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		NASAL and SINUS DECONGESTANT	openfda.brand_name
generic name		PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		JHK Inc dba American Safety & First Aid	openfda.manufacturer_name
ndc	package	73598-1264-1	openfda.package_ndc
ndc	package	73598-1262-1	openfda.package_ndc
ndc	product	73598-1262	openfda.product_ndc
ndc	product	73598-1264	openfda.product_ndc
ndc11	package	73598126201	derived:openfda.package_ndc
ndc11	package	73598126401	derived:openfda.package_ndc
rxcui		1299145	openfda.rxcui
spl id		050efff2-4886-4c50-a92c-3f216d200e8a	id
spl set id		63e51305-2575-49c4-9fda-7b3e1b4b6ede	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 an MAOI drug. If you do not know if your prescription drug contains an MAOI, consult a doctor or pharmacist before taking this product. Ask a doctor before use if you have liver disease heart disease high blood pressure thyroid disease diabetes trouble urinating due to an enlarged prostate gland When using this product do not exceed recommended dose Stop use and ask a doctor if nervousness, dizziness or sleeplessness occur symptoms do not improve within 7 days or are accompanied by fever new symptoms occur 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.