Redicare 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: Redicare Nasal and Sinus Decongestant
Generic name: REDICARE NASAL AND SINUS DECONGESTANT
Manufacturer: Redicare LLC
Product type: HUMAN OTC DRUG
SPL set ID: 2f24be68-f30e-d916-e063-6294a90a7e31
SPL ID: 2f85be59-0ea7-285b-e063-6294a90a2aa5
Version: 2
Effective date: 2025-03-04
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 05:57:32

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		Redicare Nasal and Sinus Decongestant	openfda.brand_name
generic name		REDICARE NASAL AND SINUS DECONGESTANT	openfda.generic_name
manufacturer name		Redicare LLC	openfda.manufacturer_name
ndc	package	71105-272-02	openfda.package_ndc
ndc	package	71105-272-01	openfda.package_ndc
ndc	product	71105-272	openfda.product_ndc
ndc11	package	71105027201	derived:openfda.package_ndc
ndc11	package	71105027202	derived:openfda.package_ndc
rxcui		1049182	openfda.rxcui
spl id		2f85be59-0ea7-285b-e063-6294a90a2aa5	id
spl set id		2f24be68-f30e-d916-e063-6294a90a7e31	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 an 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 (1-800-222-1222) right away.

Reported adverse events (FAERS/openFDA)#

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