Dosage and administration
Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.
Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.
Brosimum acutifolium bark 32X, Himatanthus sucuuba bark 32X, Mansoa alliacea bark and leaf 32X, Minquartia guianenis bark 32X, Phyllanthus niruri whole herb 32X, Piper aduncum leaf 32X.
For temporary relief of symptoms of musculoskeletal discomfort.
If pregnant or breast-feeding, ask a health professional before use. Consult a physician for use in children under 12 years of age.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.
Adults and children 10 drops under the tongue, twice daily or as directed. If symptoms persist, consult your health care professional.
Demineralized water, 25% Ethanol
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
For temporary relief of symptoms of musculoskeletal discomfort.
Distributed by
Chi Research, Inc.
207 6th Street South
Walker, MN 56484
218-547-1775
CHI
RESEARCH
SP
Homeopathic Remedy
4 fl. oz. (120 ml)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52654-0003-1 | 2022-11-11 | C162847 | 48780-1 | 9d75b9cf-e99f-f424-e053-dadaa90a57ce | Drug Facts: |
| 52654-0003-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-e99f-f424-e053-dadaa90a57ce | Drug Facts: |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BROSIMUM ACUTIFOLIUM BARK | ACTIVE INGREDIENT | 8Q6X4504YC | 1 | |
| HIMATANTHUS LANCIFOLIUS BARK | ACTIVE INGREDIENT | 8O169FEF9T | 1 | |
| MANSOA ALLIACEA BARK | ACTIVE INGREDIENT | 2H997JHQ75 | 1 | |
| MANSOA ALLIACEA LEAF | ACTIVE INGREDIENT | 63AYO2O03Y | 1 | |
| MINQUARTIA GUIANENSIS BARK | ACTIVE INGREDIENT | 8Q29UL9T9Z | 1 | |
| PHYLLANTHUS NIRURI WHOLE | ACTIVE INGREDIENT | NSN3MQO38G | 1 | |
| PIPER ADUNCUM LEAF | ACTIVE INGREDIENT | 718MWR54QO | 1 | |
| BROSIMUM ACUTIFOLIUM BARK | ACTIVE MOIETY | 8Q6X4504YC | 1 | |
| HIMATANTHUS LANCIFOLIUS BARK | ACTIVE MOIETY | 8O169FEF9T | 1 | |
| MANSOA ALLIACEA BARK | ACTIVE MOIETY | 2H997JHQ75 | 1 | |
| MANSOA ALLIACEA LEAF | ACTIVE MOIETY | 63AYO2O03Y | 1 | |
| MINQUARTIA GUIANENSIS BARK | ACTIVE MOIETY | 8Q29UL9T9Z | 1 | |
| PHYLLANTHUS NIRURI WHOLE | ACTIVE MOIETY | NSN3MQO38G | 1 | |
| PIPER ADUNCUM LEAF | ACTIVE MOIETY | 718MWR54QO | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 52654-0003 | 52654-0003-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BROSIMUM ACUTIFOLIUM BARK | 8Q6X4504YC | ACTIM |
| HIMATANTHUS LANCIFOLIUS BARK | 8O169FEF9T | ACTIB |
| MANSOA ALLIACEA BARK | 2H997JHQ75 | ACTIB |
| MANSOA ALLIACEA LEAF | 63AYO2O03Y | ACTIB |
| MINQUARTIA GUIANENSIS BARK | 8Q29UL9T9Z | ACTIB |
| PHYLLANTHUS NIRURI WHOLE | NSN3MQO38G | ACTIB |
| PIPER ADUNCUM LEAF | 718MWR54QO | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | 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 | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml |
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 |
|---|---|---|---|---|---|---|
| 05096613-11bb-460f-95ca-cc4e79e980c8 | 92232197-e152-4d06-8681-590eef1a76e7 | 2022-11-11 | Warnings | 05096613-11bb-460f-95ca-cc4e79e980c8 92232197-e152-4d06-8681-590eef1a76e7 |
Adverse event summaries are temporarily unavailable. Other product information remains available.