Sinus Relief

Manufacturer
Similasan Corporation
Effective date
2017-04-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:08:40

Label at a glance#

ProductSinus Relief
Active ingredientPOTASSIUM DICHROMATE, LUFFA OPERCULATA FRUIT, SCHOENOCAULON OFFICINALE SEED
Label structure10 sections

Indications and uses

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as: • Runny nose due to colds • Sinus pressure • Nasal congestion • Post-nasal drip • Irritating dryness of nasal passages

Dosage and administration

For adults and children ages 2 and over: • Remove tamper-evident plastic seal from bottle. • Lift cap off bottle. • Spray 1-3 times into each nostril. • Use as needed. • Replace cap after use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

SINUS RELIEF

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Kali bichromicum 6X

Luffa operculata 6X

Sabadilla 6X

Purpose

OTC - PURPOSE SECTION

sinus congestion, runny nose, sinus pressure, nasal dryness

runny nose, nasal dryness, sinus congestion

sneezing, itching

Uses*

INDICATIONS & USAGE SECTION

According to homeopathic principles, the active ingredients in this product temporarily relieve minor symptoms such as:

• Runny nose due to colds

• Sinus pressure

• Nasal congestion

• Post-nasal drip

• Irritating dryness of nasal passages

Warnings

WARNINGS SECTION

• According to homeopathic principles, symptoms may temporarily worsen before improving (Initial exacerbation of symptoms).

• Replace cap tightly after every use.

• To avoid contamination, do not touch the tip of the container to any surface besides nose.

• Discard open bottle after 6 months.

• The use of this container by more than one person may spread infection.

If pregnant, trying to get pregnant or breast feeding, ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Ask a doctor before use if you:

OTC - ASK DOCTOR SECTION

• Are susceptible to nose bleeds.

• Are prone to ear, nose or throat sensitivity.

Stop use and ask a doctor if:

OTC - STOP USE SECTION

• symptoms worsen or persist for more than 72 hours

Directions

DOSAGE & ADMINISTRATION SECTION

For adults and children ages 2 and over:

• Remove tamper-evident plastic seal from bottle.

• Lift cap off bottle.

• Spray 1-3 times into each nostril.

• Use as needed.

• Replace cap after use.

Other Information

OTHER SAFETY INFORMATION

Active ingredients are manufactured according to homeopathic principles.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water, Sodium chloride

Questions?

OTC - QUESTIONS SECTION

Reach our representatives at 1-800-240-9780 or getinfo@similasanusa.com.

www.SimilasanUSA.com

*These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 59262-243-20
Similasan
Sinus
Relief
20 mL/ 0.68 fl oz

NDC 59262-243-20 Similasan Sinus Relief 20 mL/ 0.68 fl ozNDC 59262-243-20 Similasan Sinus Relief 20 mL/ 0.68 fl oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59262-243-202020-01-31C16284748780-19d75b9d0-831a-f424-e053-dadaa90a57ceSinus Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59262-243-20Sinus Relief20 mL in 1 BOTTLE, SPRAYSPRAY201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59262-243SINUS RELIEF (POTASSIUM DICHROMATE, LUFFA OPERCULATA FRUIT AND SCHOENOCAULON OFFICINALE SEED) SPRAY [SIMILASAN CORPORATION]1Legacy NDC, 1 package rows20170501_57a02104-53d8-4d36-80f9-4fec891deeb2.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59262-24359262-243-20

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2b6a0e33-9486-438d-82ee-bf520b2ce91157a02104-53d8-4d36-80f9-4fec891deeb22017-04-04WarningsExact identifier
spl id: 2b6a0e33-9486-438d-82ee-bf520b2ce911
spl set id: 57a02104-53d8-4d36-80f9-4fec891deeb2

Reported adverse events (FAERS/openFDA)#

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