Rhinodol Nasal Spray

Manufacturer
New Leaf Pharmaceutical, LLC
Effective date
2019-09-27
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 02:11:30

Label at a glance#

ProductRhinodol
Active ingredientCAPSICUM
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Capsicum Anuum Fruit Extract 5x HPUS

"HPUS" indicates the active ingredients are in the official Homeopathic Pharmacopeia of the United States.

OTC - PURPOSE SECTION

Purpose:

For the relief of pain (head, extremities), anxiety, insomnia, myalgia, congestion

INDICATIONS & USAGE SECTION

Uses:

Temporarily relieves the symptoms of pain and inflammation in the head and extremities. Relieves nervousness and anxiety, insomnia, myalgia, congestion, fever.

WARNINGS SECTION

Warnings:

As with any drug, ask a doctor before use if pregnant or breastfeeding, or if allergic to any of the ingredients do not use. Consult a physician if your symptoms persist or worsen.

DOSAGE & ADMINISTRATION SECTION

Facts:

1 spray in each nostril (2 total sprays)

500 mcg

Sprays per container 114

INSTRUCTIONS FOR USE SECTION

Directions:

Adults 18 yrs. or older unless directed by physician.

Shake bottle well before each use. Spray one metered dose into each nostril.

Serving Size: 1 spray in each nostril

Use up to 3x per day.

INACTIVE INGREDIENT SECTION

Other Ingredients:

Purified water, Patented Nano-Silver (natural preservative), Nano Emulsified CBD (from organic hemp; contains no THC), Aloe Vera Extract, Eucalyptol, Rosemary Extract, Sea Salt (sodium chloride), Xanthan Gum and Vitamin C (Ascorbic Acid).

This Nanoemulsion increases bioavailability up to 10x greater than other CBD products.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of the reach of children. In case of accidental overdose, contact a medical professional or a poison control center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rhinodol CBDRhinodol CBD

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71798-015-022021-01-29C16284748780-1ba0f9c33-4039-a910-e053-dadaa90a0b85Rhinodol Nasal Spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71798-015-02Rhinodol1 in 1 BOXSPRAY111
71798-015-02Rhinodol15 mL in 1 BOTTLE, SPRAYSPRAY1511

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71798-015RHINODOL (CAPSICUM ANUUM FRUIT EXTRACT) SPRAY [NEW LEAF PHARMACEUTICAL, LLC]11Legacy NDC, 2 package rows20190928_5991bb5f-a325-6c5d-e053-2a91aa0a3bee.zip

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
71798-01571798-015-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
9390cef5-23a2-023d-e053-2995a90a4cf15991bb5f-a325-6c5d-e053-2a91aa0a3bee2019-09-27WarningsExact identifier
spl id: 9390cef5-23a2-023d-e053-2995a90a4cf1
spl set id: 5991bb5f-a325-6c5d-e053-2a91aa0a3bee

Reported adverse events (FAERS/openFDA)#

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