ValuMeds Nasal Decongestant PE Phenylephrine

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 PE Phenylephrine
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Cabinet Health P.B.C.
Product type: HUMAN OTC DRUG
SPL set ID: 3f284420-87c1-4c17-99e5-bc569bf9d45f
SPL ID: 5644bd60-9db9-e49a-e063-6394a90a3348
Version: 1
Effective date: 2026-07-10
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 05:56:35

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 PE Phenylephrine	openfda.brand_name
generic name		PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Cabinet Health P.B.C.	openfda.manufacturer_name
ndc	package	82725-1011-1	openfda.package_ndc
ndc	package	82725-1011-2	openfda.package_ndc
ndc	product	82725-1011	openfda.product_ndc
ndc11	package	82725101101	derived:openfda.package_ndc
ndc11	package	82725101102	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		5644bd60-9db9-e49a-e063-6394a90a3348	id
spl set id		3f284420-87c1-4c17-99e5-bc569bf9d45f	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 hav 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.