FDA.reportPublic FDA data

Sinus Relief

Manufacturer
Homeocare Laboratories
Effective date
2018-12-31
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:11:04

Label at a glance#

ProductSinus Relief
Active ingredientASAFETIDA, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LUFFA OPERCULATA WHOLE, SILICON DIOXIDE, SINUSITISINUM
Label structure8 sections

Label contents#

Full prescribing information#

Active ingredients:

OTC - ACTIVE INGREDIENT SECTION

Asafoetida 8X, Echinacea angustifolia 12X, Hepar sulph. 8X, Kali bic. 18X, Luffa operculata 9C, Silicea 10X, Sinusitisinum 18X.

Inactive ingredients:

INACTIVE INGREDIENT SECTION

Sucrose/lactose.

Purpose:

OTC - PURPOSE SECTION

For the temporary relief of sinus pain and inflammation.

Warnings:

WARNINGS SECTION

If symptoms persist or worsen, or if pregnant or nursing, consult a doctor. Keep out of reach of children. Do not use if cap seal is broken or missing.

Indications & Usage:

INDICATIONS & USAGE SECTION

Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Dosage & Administration:

DOSAGE & ADMINISTRATION SECTION

Turn tube upside down, twist cap to break seal & release pellets. Using clear cap, place 3 pellets to dissolve under your tongue 3 times a day or as needed. Take apart from food or drinks. To preserve purity avoid touching pellets with fingers.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Sinus Relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sinus Relief

Homeopathic Medicine

85 Pellets

SINUS-RELIEF.jpg

sinus relief imagesinus relief image

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61727-335-21Sinus Relief4 g in 1 TUBEPELLET43

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
61727-335SINUS RELIEF (ASAFETIDA, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LUFFA OPERCULATA WHOLE, SILICON DIOXIDE, SINUSITISINUM) PELLET [HOMEOCARE LABORATORIES]3Current NDC, Legacy NDC, 1 package rows20190312_84483171-df92-47de-9203-ed02d64fb5fb.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ASAFETIDAACTIVE INGREDIENTW9FZA51AS11
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51Q1
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US81
LUFFA OPERCULATA WHOLEACTIVE INGREDIENTT013HM08S01
POTASSIUM DICHROMATEACTIVE INGREDIENTT4423S18FM1
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU41
SINUSITISINUMACTIVE INGREDIENTB575563DM51
ASAFETIDAACTIVE MOIETYW9FZA51AS11
CALCIUM SULFIDEACTIVE MOIETY1MBW07J51Q1
DICHROMATE IONACTIVE MOIETY9LKY4BFN2V1
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US81
LUFFA OPERCULATA WHOLEACTIVE MOIETYT013HM08S01
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU41
SINUSITISINUMACTIVE MOIETYB575563DM51
LACTOSEINACTIVE INGREDIENTJ2B2A4N98G1
SUCROSEINACTIVE INGREDIENTC151H8M5541

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61727-33561727-335-21

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
SUCROSEC151H8M554IACT
LACTOSEJ2B2A4N98GIACT
ASAFETIDAW9FZA51AS1ACTIB
ECHINACEA ANGUSTIFOLIAVB06AV5US8ACTIB
CALCIUM SULFIDE1MBW07J51QACTIB
POTASSIUM DICHROMATET4423S18FMACTIB
LUFFA OPERCULATA WHOLET013HM08S0ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SINUSITISINUMB575563DM5ACTIB

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
LACTOSELACTOSEJ2B2A4N98GTABLET / SUBLINGUAL352 mgExact identifier — unii+route
2 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii+route
2 equally ranked IID candidates
SUCROSESUCROSEC151H8M554TABLET / SUBLINGUAL109 mgExact identifier — unii+route
2 equally ranked IID candidates
LACTOSELACTOSEJ2B2A4N98GTABLET / SUBLINGUAL352 mgExact identifier — unii+route
2 equally ranked IID candidates

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sinus ReliefASAFETIDA, ECHINACEA ANGUSTIFOLIA, CALCIUM SULFIDE, POTASSIUM DICHROMATE, LUFFA OPERCULATA WHOLE, SILICON DIOXIDE, SINUSITISINUMHomeocare Laboratories84483171-df92-47de-9203-ed02d64fb5fb2018-12-31WarningsExact identifier
ndc (package): 61727-335-21
ndc (product): 61727-335
ndc11 (package): 61727033521
spl id: 7e58bc5a-9e06-3e20-e053-2991aa0a4d35
spl set id: 84483171-df92-47de-9203-ed02d64fb5fb

Reported adverse events (FAERS/openFDA)#

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