OTC - ACTIVE INGREDIENT SECTION
| Ingredients: | |
|---|---|
| Acidum nitricum | 4X |
| Acidum sulfuricum | 4X |
| Gratiola officinalis | 4X |
| Hydrastis canadensis | 4X |
| Lachesis muta | 7X |
| Lytta vesicatoria (Cantharis) | 4X |
| Bellis perennis | 1X |
| Glechoma hederacea | 16.02 mg/ml |
| Ingredients: | |
|---|---|
| Acidum nitricum | 4X |
| Acidum sulfuricum | 4X |
| Gratiola officinalis | 4X |
| Hydrastis canadensis | 4X |
| Lachesis muta | 7X |
| Lytta vesicatoria (Cantharis) | 4X |
| Bellis perennis | 1X |
| Glechoma hederacea | 16.02 mg/ml |
Selected ingredients prepared by spagyric processes.
Contains 25% alcohol by volume.
Supports the relief of inflammation of the mucosa. Application of this homeopathic remedy for the designated usage is exclusively based on homeopathic experience. With severe forms of this disease, a clinically proven therapy is indicated.
Unless otherwise prescribed, adults take 15-20 drops, 3 times per day. For pediatric dosages, consult your practitioner.
If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use.
Keep out of the reach of children.
Protect from light and heat.
Do not use this product if tamper evident strip is broken or removed from base of cap.
To report adverse events, contact BioResource at 321B Blodgett Street, Cotati, CA 94931
Manufactured by:
PEKANA®
GmbH
D-88353 Kisslegg
Distributed by:
BioResource Inc.
Cotati, CA 94931
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| bellis perennis | ACTIVE INGREDIENT | 2HU33I03UY | 1 | |
| glechoma hederacea | ACTIVE INGREDIENT | L6O7WQK912 | 1 | |
| goldenseal | ACTIVE INGREDIENT | ZW3Z11D0JV | 1 | |
| gratiola officinalis | ACTIVE INGREDIENT | BDD9991A36 | 1 | |
| lachesis muta venom | ACTIVE INGREDIENT | VSW71SS07I | 1 | |
| lytta vesicatoria | ACTIVE INGREDIENT | 3Q034RO3BT | 1 | |
| nitric acid | ACTIVE INGREDIENT | 411VRN1TV4 | 1 | |
| sulfuric acid | ACTIVE INGREDIENT | O40UQP6WCF | 1 | |
| bellis perennis | ACTIVE MOIETY | 2HU33I03UY | 1 | |
| glechoma hederacea | ACTIVE MOIETY | L6O7WQK912 | 1 | |
| goldenseal | ACTIVE MOIETY | ZW3Z11D0JV | 1 | |
| gratiola officinalis | ACTIVE MOIETY | BDD9991A36 | 1 | |
| lachesis muta venom | ACTIVE MOIETY | VSW71SS07I | 1 | |
| lytta vesicatoria | ACTIVE MOIETY | 3Q034RO3BT | 1 | |
| nitric acid | ACTIVE MOIETY | 411VRN1TV4 | 1 | |
| sulfuric acid | ACTIVE MOIETY | O40UQP6WCF | 1 | |
| alcohol | INACTIVE INGREDIENT | 3K9958V90M | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 59469-171 | 59469-171-40 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Silver Nitrate | 95IT3W8JZE | ACTIB |
| Sulfuric Acid | O40UQP6WCF | ACTIB |
| Bellis Perennis | 2HU33I03UY | ACTIB |
| Lytta vesicatoria | 3Q034RO3BT | ACTIB |
| Gratiola officinalis | BDD9991A36 | ACTIB |
| Goldenseal | ZW3Z11D0JV | ACTIB |
| Lachesis Muta Venom | VSW71SS07I | ACTIB |
| Glechoma hederacea Flowering Top | 2458J91U39 | 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 / INTRAVENOUS | 92 %w/v | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 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 |
|---|---|---|---|---|---|---|
| 570ff30b-85ac-427f-819c-9b61b05c523a | 8b79b6e7-2079-4d27-b96a-cd57a8535be2 | 2019-11-18 | Warnings | 8b79b6e7-2079-4d27-b96a-cd57a8535be2 |
Adverse event summaries are temporarily unavailable. Other product information remains available.