FDA.reportPublic FDA data

YSNORE Anti-Snoring Nasal Pump Spray 10ml

Manufacturer
Y Snore
Effective date
2018-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:09:08

Label at a glance#

ProductYSNORE
Active ingredientDIOSCOREA VILLOSA ROOT, GINGER
Label structure10 sections

Indications and uses

Clinically proven to reduce or stop the symptoms of snoring.

Dosage and administration

Use only as directed • Shake well before use. • With head upright 1 or 2 sprays at the base of each nostril prior to sleep. • Store at room temperature not to exceed 80° F. • For individual use only. • For best results daily use is required.

Label contents#

Full prescribing information#

Homeopathic Purpose

OTC - ACTIVE INGREDIENT SECTION

Active IngredientsPurpose
Dioscorea Villosa 2x HPUSReduces irritation of nasal Passages
Zingiber Officianle 2x HPUS....

Uses

INDICATIONS & USAGE SECTION

Clinically proven to reduce or stop the symptoms of snoring.

Warnings

WARNINGS SECTION

• Do not use on children under 12 years of age.

OTC - PREGNANCY OR BREAST FEEDING SECTION

• If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

• This product is not intended to treat sleep apnea. See a physician if symptoms of sleep apnea occur.

OTC - STOP USE SECTION

• Stop use and ask a physician if symptoms do not improve in 14 days, or worsen.

Directions

DOSAGE & ADMINISTRATION SECTION

Use only as directed
• Shake well before use.
• With head upright 1 or 2 sprays at the base of each nostril prior to sleep.
• Store at room temperature not to exceed 80° F.
• For individual use only.
• For best results daily use is required.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, ethanol, glycerin, purified water, and sodium chloride.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label imageLabel image

Updated 1/9/2108

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62587-219-30YSNORE1 in 1 PACKAGESPRAY13
62587-219-30YSNORE10 mL in 1 BOTTLE, SPRAYSPRAY103

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62587-219YSNORE (DIOSCOREA VILLOSA ROOT, GINGER) SPRAY [Y SNORE]3Current NDC, Legacy NDC, 2 package rows20180110_4f0a27f1-1584-4bca-b6b8-b5cd273e7242.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DIOSCOREA VILLOSA ROOTACTIVE INGREDIENTIWY3IWX2G81
GINGERACTIVE INGREDIENTC5529G5JPQ1
DIOSCOREA VILLOSA ROOTACTIVE MOIETYIWY3IWX2G81
GINGERACTIVE MOIETYC5529G5JPQ1
ALCOHOLINACTIVE INGREDIENT3K9958V90M1
BENZALKONIUM CHLORIDEINACTIVE INGREDIENTF5UM2KM3W71
GLYCERININACTIVE INGREDIENTPDC6A3C0OX1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8X1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62587-21962587-219-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
ALCOHOL3K9958V90MIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
DIOSCOREA VILLOSA ROOTIWY3IWX2G8ACTIB
GINGERC5529G5JPQACTIB

Source Document#

Source XML

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 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSPRAY / NASAL30 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSPRAY / NASAL22.3 mg/1mlExact identifier — unii+route+dosage form
2 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SPRAY / NASAL1 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
BENZALKONIUM CHLORIDEBENZALKONIUM CHLORIDEF5UM2KM3W7SPRAY / NASAL1 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
SODIUM CHLORIDESODIUM CHLORIDE451W47IQ8XSPRAY / NASAL30 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
GLYCERINGLYCERINPDC6A3C0OXSPRAY / NASAL22.3 mg/1mlExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii+route+dosage form
2 equally ranked IID candidates
ALCOHOLALCOHOL3K9958V90MSPRAY / NASAL20 mgExact identifier — unii+route+dosage form
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
YSNOREDIOSCOREA VILLOSA ROOT, GINGERY Snore4f0a27f1-1584-4bca-b6b8-b5cd273e72422018-01-09WarningsExact identifier
ndc (package): 62587-219-30
ndc (product): 62587-219
ndc11 (package): 62587021930
spl id: 62609808-7a83-1785-e053-2991aa0aaac3
spl set id: 4f0a27f1-1584-4bca-b6b8-b5cd273e7242

Reported adverse events (FAERS/openFDA)#

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