SINUPET

Manufacturer
Groupe Cyrenne Inc.
Effective date
2025-11-20
Label type
OTC ANIMAL DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 02:36:06

Label at a glance#

ProductSINUPET
Active ingredientONION, EUPHRASIA STRICTA, GOLDENSEAL, NAPHTHALENE, SILICON DIOXIDE, THUJA OCCIDENTALIS LEAFY TWIG, POTASSIUM DICHROMATE, PULSATILLA VULGARIS WHOLE, SOLIDAGO VIRGAUREA FLOWERING TOP, OYSTER SHELL CALCIUM CARBONATE, CRUDE
Label structure7 sections

Indications and uses

Promotes sinus and respiratory health. For cats and dogs only.

Label contents#

Full prescribing information#

Active ingredient                                         Purpose

OTC - ACTIVE INGREDIENT SECTION

Allium Cepa 30k                                         Runny nose

Euphrasia Officinalis 30k                             Sinus pain

Hydrastis Canadensis 30k                           Nasal secretions

Naphthalinum 30k                                     Abundant mucous

Pulsatilla 30k                                            Yellow discahrge

Silicea 30k                                                Suppuration

Kali Bichromicum 30k                                 Stuffy nose

Thuja Occidentalis 30k                                Green mucus

Calcarea Carbonica 30k                               Obstruction

Solidago 30k                                              Sneezing

Uses

INDICATIONS & USAGE SECTION

Promotes sinus and respiratory health. For cats and dogs only.

Warnings

WARNINGS SECTION

Keep out of reach of children.

Direction

DOSAGE & ADMINISTRATION SECTION

1 spray every day, in water or directly in the mouth. Stop when symptoms disappear. Not for prevention.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Ethyl alcohol 20%, purified water

Cautions

SPL UNCLASSIFIED SECTION

Shake well before use. Respect the dosage. Essential oils can negate the effects of homeopathic products. Store in a cool place away from direct sunlight.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86147-024-01SINUPET30 mL in 1 BOTTLELIQUID306

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86147-02486147-024-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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 · 10 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Allium cepaONIONBoiron84b4c3d2-9c51-ca6e-e053-2a91aa0a01032023-10-18Name fallback
generic name: ONION
Allium cepaONIONBoiron84b4dc86-77e5-333a-e053-2991aa0a4c242023-10-18Name fallback
generic name: ONION
Allium cepaONIONBoiron84ed21a8-01e3-2480-e053-2a91aa0a9ce42023-10-13Name fallback
generic name: ONION
Allium cepaONIONBoiron84ed9d5b-5385-7142-e053-2a91aa0a95fe2023-10-13Name fallback
generic name: ONION
Allium cepaONIONBoiron84ed9217-f2eb-4d35-e053-2a91aa0a20162023-10-13Name fallback
generic name: ONION
Allium cepaONIONBoiron84b4dc86-781a-333a-e053-2991aa0a4c242023-10-13Name fallback
generic name: ONION
Allium cepaONIONBoiron84ed9217-f2e3-4d35-e053-2a91aa0a20162023-07-11Name fallback
generic name: ONION
Allium cepaONIONBoironc18887f0-794a-11e6-8b60-424c583030312023-02-20Name fallback
generic name: ONION
Allium cepaONIONBoiron84ed787f-b68c-3aba-e053-2a91aa0a23432023-01-20Name fallback
generic name: ONION
Allium cepaONIONBoiron84edc238-e31f-071b-e053-2a91aa0a1cf22023-01-20Name fallback
generic name: ONION

Reported adverse events (FAERS/openFDA)#

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