GoodMeds 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: GoodMeds Nasal Decongestant
Generic name: PHENYLEPHRINE HYDROCHLORIDE
Manufacturer: Cabinet Health P.B.C.
Product type: HUMAN OTC DRUG
SPL set ID: 6a8a961c-d2d2-428d-8af7-8527aae25c8a
SPL ID: 54a07aed-19a7-e4a1-e063-6294a90aad22
Version: 1
Effective date: 2026-06-19
Source export date: 2026-09-28
Source partition: 6
Source file: https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:37:43

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		GoodMeds Nasal Decongestant	openfda.brand_name
generic name		PHENYLEPHRINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Cabinet Health P.B.C.	openfda.manufacturer_name
ndc	package	82725-4011-1	openfda.package_ndc
ndc	product	82725-4011	openfda.product_ndc
ndc11	package	82725401101	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		54a07aed-19a7-e4a1-e063-6294a90aad22	id
spl set id		6a8a961c-d2d2-428d-8af7-8527aae25c8a	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 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.