Naturasil
- Manufacturer
- Nature's Innovation, Inc.
- Effective date
- 2021-01-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:56:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Drug Facts
Active Ingredients:
Hypericum 6X HPUS
Arnica Montana 1X HPUS
DESCRIPTION SECTION
The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.
OTC - PURPOSE SECTION
Purpose
Neuropathy, Tingling, Burning and Numbness Symptom Relief
Muscle Pain, Neuralgia, Stiffness, Swelling, Bruising Symptom Relief
INDICATIONS & USAGE SECTION
Uses: Symptomatic treatment of neuropathy, tingling, burning and numbness.
WARNINGS SECTION
Warnings: For external use only.
OTC - ASK DOCTOR SECTION
Ask a doctor before use if pregnant or nursing.
OTHER SAFETY INFORMATION
Avoid contact with eyes.
OTC - DO NOT USE SECTION
Do Not use by mouth, in nostrils, on wounds or damaged skin.
OTC - STOP USE SECTION
Discontinue use if irritation occurs.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OTC - DO NOT USE SECTION
Do not use if tamper evident seal is broken.
OTHER SAFETY INFORMATION
In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.
DOSAGE & ADMINISTRATION SECTION
Directions: SHAKE WELL! Apply 10-20 drops and massage into areas with symptoms of neuropathy. May be used 3-4 times daily. Pain will subside in 1-4 weeks. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Cypress Leaf Oil, Eucalyptus Leaf Oil, Pelargonium Leaf Oil, Peppermint Leaf Oil, Sesame Seed Oil.
OTC - QUESTIONS SECTION
Questions? Comments?
www.naturasil.com 866.371.2499 Mfd. by: Nature's
Innovation, Inc. 2723 Brickton North Dr., Buford, GA 3058 Not tested on animals.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
NDC# 10893-350-30
100%
Natural Plant
Extracts
Naturasil
30ml (1.014 fl. oz.)
Topical Liquid
Homeopathic Medicine
Neuropathy
Rub
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ARNICA MONTANA | ACTIVE INGREDIENT | O80TY208ZW | 1 | |
| ST. JOHN'S WORT | ACTIVE INGREDIENT | UFH8805FKA | 1 | |
| ARNICA MONTANA | ACTIVE MOIETY | O80TY208ZW | 1 | |
| ST. JOHN'S WORT | ACTIVE MOIETY | UFH8805FKA | 1 | |
| CUPRESSUS SEMPERVIRENS LEAF OIL | INACTIVE INGREDIENT | M7QUY89S4O | 1 | |
| EUCALYPTUS OIL | INACTIVE INGREDIENT | 2R04ONI662 | 1 | |
| GERANIUM OIL, ALGERIAN TYPE | INACTIVE INGREDIENT | 5Q1I94P4WG | 1 | |
| JOJOBA OIL | INACTIVE INGREDIENT | 724GKU717M | 1 | |
| PEPPERMINT OIL | INACTIVE INGREDIENT | AV092KU4JH | 1 | |
| SESAME OIL | INACTIVE INGREDIENT | QX10HYY4QV | 1 |
Products#
Every source-derived product name is available through these pages.
- Naturasil Neuropathy Rub
- Hypericum and Arnica Montana
- ST. JOHN'S WORT
- ARNICA MONTANA
- CUPRESSUS SEMPERVIRENS LEAF OIL
- EUCALYPTUS OIL
- GERANIUM OIL, ALGERIAN TYPE
- JOJOBA OIL
- PEPPERMINT OIL
- SESAME OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 10893-350 | 10893-350-30 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ST. JOHN'S WORT | UFH8805FKA | ACTIB |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| CUPRESSUS SEMPERVIRENS LEAF OIL | M7QUY89S4O | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| GERANIUM OIL, ALGERIAN TYPE | 5Q1I94P4WG | IACT |
| JOJOBA OIL | 724GKU717M | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| SESAME OIL | QX10HYY4QV | IACT |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / ORAL | 526 mg | ||
| EUCALYPTUS OIL | EUCALYPTUS OIL | 2R04ONI662 | SYRUP / ORAL | NA | ||
| SESAME OIL | SESAME OIL | QX10HYY4QV | INJECTION / INTRAMUSCULAR | 70 %v/v | ||
| SESAME OIL | SESAME OIL | QX10HYY4QV | CAPSULE / ORAL | 2325 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CONCENTRATE / ORAL | 0.05 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | ELIXIR / ORAL | 0.04 mg/1ml | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / SUBLINGUAL | 0.15 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET, ORALLY DISINTEGRATING / ORAL | 3 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SHAMPOO / TOPICAL | 0.2 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | OINTMENT / TOPICAL | 0.2 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SUSPENSION / ORAL | 100 mg/1ml | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SPRAY, METERED / SUBLINGUAL | 1 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / DENTAL | 0.04 %v/v | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER / SUBLINGUAL | 1 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SOLUTION / ORAL | 53 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | PASTE, DENTIFRICE / DENTAL | 49.3 %w/w | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | GUM, CHEWING / BUCCAL | 526 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | LOZENGE / ORAL | 12 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | FILM / BUCCAL | 12 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | TABLET / ORAL | 28 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | SYRUP / ORAL | 120 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | CAPSULE / ORAL | 60 mg | ||
| PEPPERMINT OIL | PEPPERMINT OIL | AV092KU4JH | POWDER, DENTIFRICE / DENTAL | NA |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 60185d7d-54eb-4ab2-a445-09a238238df6 | 3815ec1e-4860-4c3a-ae8e-aeffd7a1a372 | 2025-07-24 | Warnings | 3815ec1e-4860-4c3a-ae8e-aeffd7a1a372 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
