ValuMeds Nasal Decongestant Phenylephrine HCl

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: ValuMeds Nasal Decongestant Phenylephrine HCl
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Cabinet Health P.B.C.
Product type: HUMAN OTC DRUG
SPL set ID: 21676b0c-6be2-464c-ae91-92e5f0d0087d
SPL ID: 42f52562-245c-9e85-e063-6294a90af104
Version: 2
Effective date: 2025-11-06
Source export date: 2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:12:54

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 · 13 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M012	openfda.application_number
brand name		ValuMeds Nasal Decongestant Phenylephrine HCl	openfda.brand_name
generic name		PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Cabinet Health P.B.C.	openfda.manufacturer_name
ndc	package	82725-1111-1	openfda.package_ndc
ndc	package	82725-1111-2	openfda.package_ndc
ndc	product	82725-1111	openfda.product_ndc
ndc11	package	82725111101	derived:openfda.package_ndc
ndc11	package	82725111102	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		42f52562-245c-9e85-e063-6294a90af104	id
spl set id		21676b0c-6be2-464c-ae91-92e5f0d0087d	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 fordepression, 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 a 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 exceed recommended dose Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur symptoms do not improve within 7 days or occur with a 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.