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.
Achyrocline satureioides whole herb 32X, Arctostaphylos uva ursi leaf 32X, Cassia occidentalis whole herb 32X, Mirabilis jalapa leaf and stem 32X, Petiveria alliacea whole herb 32X, Physalis angulata whole herb 32X, Schinus molle bark 32X.
For relief of symptoms of respiratory 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 relief of symptoms of respiratory discomfort.
Distributed by
Chi Research, Inc.
207 6th Street South
Walker, MN 56484
218-547-1775
CHI
RESEARCH
MP
Homeopathic Remedy
4 fl. oz. (120 ml)
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 52654-0001-1 | 2022-11-11 | C162847 | 48780-1 | 9d75b9cf-e99c-f424-e053-dadaa90a57ce | Drug Facts: |
| 52654-0001-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-e99c-f424-e053-dadaa90a57ce | Drug Facts: |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ACHYROCLINE SATUREIOIDES | ACTIVE INGREDIENT | PGA1AZ433Z | 1 | |
| ARCTOSTAPHYLOS UVA-URSI LEAF | ACTIVE INGREDIENT | 3M5V3D1X36 | 1 | |
| MIRABILIS JALAPA FLOWERING TOP | ACTIVE INGREDIENT | 623IWX4U2M | 1 | |
| PETIVERIA ALLIACEA WHOLE | ACTIVE INGREDIENT | 7JU9V35411 | 1 | |
| PHYSALIS ANGULATA | ACTIVE INGREDIENT | W4TKW9D5GG | 1 | |
| SCHINUS MOLLE BARK | ACTIVE INGREDIENT | 960WYU9I5Z | 1 | |
| SENNA OCCIDENTALIS | ACTIVE INGREDIENT | N4U494DYS5 | 1 | |
| ACHYROCLINE SATUREIOIDES | ACTIVE MOIETY | PGA1AZ433Z | 1 | |
| ARCTOSTAPHYLOS UVA-URSI LEAF | ACTIVE MOIETY | 3M5V3D1X36 | 1 | |
| MIRABILIS JALAPA FLOWERING TOP | ACTIVE MOIETY | 623IWX4U2M | 1 | |
| PETIVERIA ALLIACEA WHOLE | ACTIVE MOIETY | 7JU9V35411 | 1 | |
| PHYSALIS ANGULATA | ACTIVE MOIETY | W4TKW9D5GG | 1 | |
| SCHINUS MOLLE BARK | ACTIVE MOIETY | 960WYU9I5Z | 1 | |
| SENNA OCCIDENTALIS | ACTIVE MOIETY | N4U494DYS5 | 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 |
|---|---|
| 52654-0001 | 52654-0001-1 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACHYROCLINE SATUREIOIDES | PGA1AZ433Z | ACTIB |
| ARCTOSTAPHYLOS UVA-URSI LEAF | 3M5V3D1X36 | ACTIB |
| SENNA OCCIDENTALIS | N4U494DYS5 | ACTIB |
| MIRABILIS JALAPA FLOWERING TOP | 623IWX4U2M | ACTIB |
| PETIVERIA ALLIACEA WHOLE | 7JU9V35411 | ACTIB |
| PHYSALIS ANGULATA | W4TKW9D5GG | ACTIB |
| SCHINUS MOLLE BARK | 960WYU9I5Z | 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 | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 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 |
|---|---|---|---|---|---|---|
| 4a7d8678-91fc-4a07-84b8-e613d23ac512 | 6e88db05-aeb3-4a97-857c-da4dbc3ad39f | 2022-11-11 | Warnings | 4a7d8678-91fc-4a07-84b8-e613d23ac512 6e88db05-aeb3-4a97-857c-da4dbc3ad39f |
Adverse event summaries are temporarily unavailable. Other product information remains available.