Redicare Nasal and Sinus Decongestant

Manufacturer: Redicare LLC
Effective date: 2025-03-04
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:56:38

Label at a glance#

ProductRedicare Nasal and Sinus Decongestant

Active ingredientPHENYLEPHRINE HYDROCHLORIDE

Label structure10 sections

Indications and uses

■ temporarily relieves sinus congestion and pressure ■ temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies

Dosage and administration

Adults and children 12 years and over: ■ 1 tablet every 4 hours ■ do not take more than 6 tablets in 24 hours Children under 12 years: ask a doctor

Storage and handling

■ store at room temperature 20°– 25°C (68°– 77°F) ■ do not use if carton or blister unit is opened or broken [for blister]

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact1-866-561-5650

Label contents#

Full prescribing information#

Active Ingredient (in each tablet)

OTC - ACTIVE INGREDIENT SECTION

Phenylephrine HCl 10mg

Purpose

OTC - PURPOSE SECTION

Nasal decongestant

Uses:

INDICATIONS & USAGE SECTION

■ temporarily relieves sinus congestion and pressure ■ temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies

Warnings:

WARNINGS SECTION

Do not use if

OTC - DO NOT USE SECTION

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

OTC - ASK DOCTOR SECTION

■ heart disease ■ high blood pressure ■ thyroid disease ■ diabetes ■ trouble urinating due to an enlarged prostate gland

When using this product

OTC - WHEN USING SECTION

do not exceed recommended dose

Stop use and ask a doctor if

OTC - STOP USE SECTION

■ nervousness, dizziness, or sleeplessness occur ■ symptoms do not improve within 7 days or occur with a fever

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and over: ■ 1 tablet every 4 hours ■ do not take more than 6 tablets in 24 hours
Children under 12 years: ask a doctor

Other Information:

STORAGE AND HANDLING SECTION

■ store at room temperature 20°– 25°C (68°– 77°F)
■ do not use if carton or blister unit is opened or broken [for blister]

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

croscarmellose sodium, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, hypromellose, lactose, magnesium stearate, microcrystalline cellulose, Opadry Clear YS-1-7006, polyethylene glycol, propylene glycol*, silicon dioxide, titanium dioxide. *May contain this ingredient

Questions or Comments?

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Call 1-866-561-5650 Monday through Friday 9AM - 5PM

Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Image

Packet

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packet

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1049182	phenylephrine HCl 10 MG Oral Tablet	PSN	2
1049182	phenylephrine hydrochloride 10 MG Oral Tablet	SCD	2

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
PHENYLEPHRINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
e4e263da-1c53-440f-bb80-b7a575843b5a	Product name	1	20260313
d2168cac-a261-415a-9c78-3522859fa720	Product name	3	20251124
05a8cdd1-eeb8-409e-b938-0778225eca7d	Product name	4	20250221
e5b5c132-b15d-435b-9faa-2f74e5cadcf9	Product name	8	20250220
f489e8f3-5c9e-4818-b539-a73587edcfc7	Product name	2	20240229
0f7ae452-206d-4fc4-868d-56fc47074084	Product name	1	20231011
b5abe2e3-39a1-43eb-9bff-f3c1653fe3df	Product name	2	20190930
e0b6c8be-f2bd-9f86-a9fc-3ed56ffaa814	Product name	3	20150910
42f3c020-f1b3-89bc-7bdc-e1f10e680485	Product name	1	20140508
e949165d-714d-e548-2b76-0cb5def16f30	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
71105-272-01	Redicare Nasal and Sinus Decongestant	2 in 1 PACKET	TABLET	2		2
71105-272-02	Redicare Nasal and Sinus Decongestant	50 in 1 BOX	TABLET	50		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71105-272	REDICARE NASAL AND SINUS DECONGESTANT TABLET [REDICARE LLC]	2	Current NDC, 2 package rows	20250306_2f24be68-f30e-d916-e063-6294a90a7e31.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Redicare Nasal and Sinus Decongestant
SILICON DIOXIDE
FD&C RED NO. 40
PROPYLENE GLYCOL
CROSCARMELLOSE SODIUM
CELLULOSE, MICROCRYSTALLINE
PHENYLEPHRINE HYDROCHLORIDE
PHENYLEPHRINE
HYPROMELLOSES
FD&C YELLOW NO. 6
MAGNESIUM STEARATE
TITANIUM DIOXIDE
POLYETHYLENE GLYCOL, UNSPECIFIED
LACTOSE, UNSPECIFIED FORM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71105-272	71105-272-01, 71105-272-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
FD&C RED NO. 40	WZB9127XOA	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CROSCARMELLOSE SODIUM	M28OL1HH48	IACT
CELLULOSE, MICROCRYSTALLINE	OP1R32D61U	IACT
PHENYLEPHRINE HYDROCHLORIDE	04JA59TNSJ	ACTIB
HYPROMELLOSES	3NXW29V3WO	IACT
FD&C YELLOW NO. 6	H77VEI93A8	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
TITANIUM DIOXIDE	15FIX9V2JP	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT
LACTOSE, UNSPECIFIED FORM	J2B2A4N98G	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Redicare Nasal and Sinus Decongestant	REDICARE NASAL AND SINUS DECONGESTANT	Redicare LLC	2f24be68-f30e-d916-e063-6294a90a7e31	2025-03-04	Warnings	Exact identifier ndc (package): 71105-272-02 ndc (package): 71105-272-01 ndc (product): 71105-272 ndc11 (package): 71105027201 ndc11 (package): 71105027202 spl id: 2f85be59-0ea7-285b-e063-6294a90a2aa5 spl set id: 2f24be68-f30e-d916-e063-6294a90a7e31

Reported adverse events (FAERS/openFDA)#

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