Indications and uses
Uses*: Homeopathic relief of symptoms of backache pain. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses*: Homeopathic relief of symptoms of backache pain. *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Directions: chew or dissolve tablets in the mouth. For Adults and Children 12+: Take 2 tablets every 15-20 minutes up to 4 doses, then every 4 hours until symptoms subside.
HPUS Active Ingredients: Equal volumes of each ingredient in a 12C potency: Arnica, Bryonia, Cimicifuga, Hypericum, Ignatia, Kali carb, nux vom, rhus tox, ruta.
Uses*: Homeopathic relief of symptoms of backache pain.
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Warnings: If symptoms persist or worsen, consult a healthcare professional. If pregnant or breastfeeding, ask a healthcare professional before use. keep this and all medication out of reach of children. In case of overdose, get medical help or contacta Poison Control Center right away.
Directions: chew or dissolve tablets in the mouth. For Adults and Children 12+: Take 2 tablets every 15-20 minutes up to 4 doses, then every 4 hours until symptoms subside.
Contains no artificial flavors or colorants. No gluten added. Lactose Free.
Tamper resistsant for your protection. use only if saftey seal is intact.
Inactive Ingredients: Magnesium Stearate, Maltodextrin, Sucrose.
Keep this and all medication out of reach of children.
If pregnant or breastfeeding, ask a health professional before use.
Temporarily relieves symptoms of backache pain.*
*claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 68703-373-80 | 2023-12-26 | C162847 | 48780-1 | f386c649-cc18-0266-e053-dadaa90a7c1a | NativeRemedies® Backache Ease Tablets |
| 68703-373-80 | 2023-01-30 | C162847 | 48780-1 | f386c649-cc18-0266-e053-dadaa90a7c1a | NativeRemedies® Backache Ease Tablets |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68703-373-80 | NativeRemedies Backache Ease | 180 in 1 BOTTLE, GLASS | TABLET | 180 | 4 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 68703-373 | NATIVEREMEDIES BACKACHE EASE (ARNICA, BRYONIA, CIMICIFUGA, HYPERICUM, IGNATIA, KALI CARB, NUX VOM, RHUS TOX, RUTA) TABLET [SILVER STAR BRANDS] | 4 | Current NDC, Legacy NDC, 1 package rows | 20250103_c6259789-438a-211a-e053-2995a90aa5c4.zip |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 68703-373 | 68703-373-80 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| RUTA GRAVEOLENS FLOWERING TOP | N94C2U587S | ACTIB |
| HYPERICUM PERFORATUM | XK4IUX8MNB | ACTIB |
| STRYCHNOS NUX-VOMICA SEED | 269XH13919 | ACTIB |
| ARNICA ANGUSTIFOLIA FLOWER | NG0U89QRD8 | ACTIB |
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| POTASSIUM CARBONATE | BQN1B9B9HA | ACTIB |
| STRYCHNOS IGNATII SEED | 1NM3M2487K | ACTIB |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| ACTAEA CIMICIFUGA ROOT | 65J267BAZT | ACTIB |
| TOXICODENDRON RADICANS LEAF | CDH3461U7L | ACTIB |
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 |
|---|---|---|---|---|---|---|
| NativeRemedies Backache Ease | ARNICA, BRYONIA, CIMICIFUGA, HYPERICUM, IGNATIA, KALI CARB, NUX VOM, RHUS TOX, RUTA | Silver Star Brands | c6259789-438a-211a-e053-2995a90aa5c4 | 2025-01-01 | Warnings | 68703-373-80 68703-373 68703037380 2ab0efa0-68e4-1b30-e063-6294a90ae73e c6259789-438a-211a-e053-2995a90aa5c4 |
Adverse event summaries are temporarily unavailable. Other product information remains available.