Indications and uses
For temporary relief of discomfort associated with lymphatic swelling and edema. These statements have not been evaluated by the Food and Drug Administration. They are supported by traditional homeopathic principles.
For temporary relief of discomfort associated with lymphatic swelling and edema. These statements have not been evaluated by the Food and Drug Administration. They are supported by traditional homeopathic principles.
Adults and children over 12 years of age: Take 20 drops in water 3 times daily. Consult a physician for use in children under 12 years of age. Do not use for children under 1 year of age.
Store at 68 to 77 °F. Tamper Evident: Do not use if tamper evident strip is broken or missing from base of bottle cap. To report serious adverse events, call 1-855-387-6466.
Drug Facts
For temporary relief of discomfort associated with lymphatic swelling and edema.
These statements have not been evaluated by the Food and Drug Administration. They are supported by traditional homeopathic principles.
For oral use only.
Chronically enlarged lymph nodes can be the sign of different diseases. Therefore, consult a doctor in order to clarify the underlying disease before using this medicine. Also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment.
Do not use if
Stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.
If pregnant or breast-feeding, ask a health professional before use.
Keep this and all medicines out of reach of children.
In case of accidental overdose, seek professional assistance or contact a poison control center immediately.
46 % ethanol V/V, purified water
1-855-387-6466
Distributed by:
Hevert Pharmaceuticals, LLC
Eugene, OR 97401
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Arsenic Trioxide | ACTIVE INGREDIENT | S7V92P67HO | 3 | |
| Clematis Recta Flowering top | ACTIVE INGREDIENT | 396421SP9F | 3 | |
| Conium Maculatum Flowering Top | ACTIVE INGREDIENT | Q28R5GF371 | 3 | |
| Lachesis Muta Venom | ACTIVE INGREDIENT | VSW71SS07I | 3 | |
| Mercuric Iodide | ACTIVE INGREDIENT | R03O05RB0P | 3 | |
| Phytolacca Americana Root | ACTIVE INGREDIENT | 11E6VI8VEG | 3 | |
| Scrophularia Nodosa | ACTIVE INGREDIENT | 7H443NUB2T | 3 | |
| Sulfur | ACTIVE INGREDIENT | 70FD1KFU70 | 3 | |
| Toxicodendron Pubescens Leaf | ACTIVE INGREDIENT | 6IO182RP7A | 3 | |
| Arsenic Cation (3+) | ACTIVE MOIETY | C96613F5AV | 3 | |
| Clematis Recta Flowering top | ACTIVE MOIETY | 396421SP9F | 3 | |
| Conium Maculatum Flowering Top | ACTIVE MOIETY | Q28R5GF371 | 3 | |
| Lachesis Muta Venom | ACTIVE MOIETY | VSW71SS07I | 3 | |
| Mercuric Iodide | ACTIVE MOIETY | R03O05RB0P | 3 | |
| Phytolacca Americana Root | ACTIVE MOIETY | 11E6VI8VEG | 3 | |
| Scrophularia Nodosa | ACTIVE MOIETY | 7H443NUB2T | 3 | |
| Sulfur | ACTIVE MOIETY | 70FD1KFU70 | 3 | |
| Toxicodendron Pubescens Leaf | ACTIVE MOIETY | 6IO182RP7A | 3 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 3 | |
| Water | INACTIVE INGREDIENT | 059QF0KO0R | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 54532-0021 | 54532-0021-5 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Arsenic Trioxide | S7V92P67HO | ACTIB |
| Clematis Recta Flowering top | 396421SP9F | ACTIB |
| Conium Maculatum Flowering Top | Q28R5GF371 | ACTIB |
| Lachesis Muta Venom | VSW71SS07I | ACTIB |
| Mercuric Iodide | R03O05RB0P | ACTIB |
| Phytolacca Americana Root | 11E6VI8VEG | ACTIB |
| Toxicodendron Pubescens Leaf | 6IO182RP7A | ACTIB |
| Scrophularia Nodosa | 7H443NUB2T | ACTIB |
| Sulfur | 70FD1KFU70 | ACTIB |
| Alcohol | 3K9958V90M | IACT |
| Water | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg |
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 |
|---|---|---|---|---|---|---|
| 26c901ad-d54d-48bf-8860-d183bc0c2203 | bfdb7aaf-d4f6-4498-b02e-d9cd500c9f4e | 2018-09-17 | Warnings | 26c901ad-d54d-48bf-8860-d183bc0c2203 bfdb7aaf-d4f6-4498-b02e-d9cd500c9f4e |
Adverse event summaries are temporarily unavailable. Other product information remains available.