Indications and uses
Homeopathic remedy temporarily relieves burning, tingling, and numbness in hands and feet.
NeuropathEase
- Manufacturer
- Silver Star Brands | King Bio
- Effective date
- 2016-04-01
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:25:20
Label at a glance#
ProductNeuropathEase
Active ingredientAMANITA MUSCARIA FRUITING BODY, HYPERICUM PERFORATUM, SILICON DIOXIDE, PHOSPHORUS, ARSENIC TRIOXIDE
Label structure10 sections
Dosage and administration
Take approximately 30 minutes before or after food. Acute: Take 0.25 mL to 0.50 mL every hour for up to 6 doses or until symptoms subside. Chronic (daily use): Take 0.25mL to 0.50 mL 2-3 times a day.
Contacts and useful links#
Websitewww.nativeremedies.com
www.nativeremedies.com
www.nativeremedies.comLabel contents#
Full prescribing information#
HPUS Active Ingredients
Each does contains equal parts of: Agaricus muscarius 30C, Arsenicum album 30C, Hypericum perforatum 30C, Phosphorus 30C, Silicea 6C.
Uses
Homeopathic remedy temporarily relieves burning, tingling, and numbness in hands and feet.
Warnings
If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medication out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
Take approximately 30 minutes before or after food. Acute: Take 0.25 mL to 0.50 mL every hour for up to 6 doses or until symptoms subside. Chronic (daily use): Take 0.25mL to 0.50 mL 2-3 times a day.
Other Information
All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com
Contains no artificial flavors or artificial colors. No gluten added.
Inactive Ingredients
Citric acid, potassium sorbate, purified water.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep this and all medication out of reach of children.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breastfeeding, ask a health professional before use.
OTC - PURPOSE SECTION
Temporarily relieves burning, tingling, & numbness in hands & feet
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68703-255-02 | 2020-02-11 | C162847 | 48780-1 | 9d75b9d0-fc2e-f424-e053-dadaa90a57ce | NativeRemedies® NeuropathEase™ |
| 68703-255-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-fc2e-f424-e053-dadaa90a57ce | NativeRemedies® NeuropathEase™ |
Products#
Every source-derived product name is available through these pages.
- NeuropathEase
- Agaricus muscarius, Arsenicum album, Hypericum perforatum, Phosphorus, Silicea
- AMANITA MUSCARIA FRUITING BODY
- HYPERICUM PERFORATUM
- SILICON DIOXIDE
- ANHYDROUS CITRIC ACID
- POTASSIUM SORBATE
- WATER
- PHOSPHORUS
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 68703-255 | 68703-255-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AMANITA MUSCARIA FRUITING BODY | DIF093I037 | ACTIB |
| HYPERICUM PERFORATUM | XK4IUX8MNB | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| ANHYDROUS CITRIC ACID | XF417D3PSL | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| WATER | 059QF0KO0R | IACT |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| ARSENIC TRIOXIDE | S7V92P67HO | ACTIB |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 2868b1de-67cd-3324-e063-6394a90a7ad8 | 2f6f6269-c188-400c-e054-00144ff88e88 | 2024-12-03 | Warnings | 2f6f6269-c188-400c-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.