Dosage and administration
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Bronchial Cough
- Manufacturer
- Deseret Biologicals, Inc. | Apotheca Company
- Effective date
- 2021-08-03
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:39:02
Label at a glance#
ProductBronchial Cough
Active ingredientPROTORTONIA CACTI, DROSERA ROTUNDIFOLIA, DRIMIA MARITIMA BULB, LOBARIA PULMONARIA, CAUSTICUM, CUPRIC ACETATE, ARSENIC TRIIODIDE, ACTIVATED CHARCOAL, POTASSIUM CARBONATE, LACHESIS MUTA VENOM
Label structure9 sections
Contacts and useful links#
Websitewww.desbio.com
www.desbio.com
www.desbio.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Coccus Cacti 4X, Drosera (Rotundifolia) 4X, Scilla Maritima 4X, Sticta Pulmonaria 4X, Causticum 6X, Cuprum Aceticum 6X, Arsenicum Iodatum 8X, Carbo Vegetabilis 12X, Kali Carbonicum 12X, Lachesis Mutus 12X.
HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to bronchial cough including irritating cough and congestion.**
** These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
WARNINGS:
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.
If pregnant or breast-feeding, ask a health professional before use.
Tamper seal: "Sealed for Your Protection."
Do not use if seal is broken or missing.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.
DIRECTIONS:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to bronchial cough including irritating cough and congestion.**
** These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
INACTIVE INGREDIENTS:
Demineralized Water, 25% Ethanol
QUESTIONS:
Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070 www.desbio.com
PACKAGE LABEL DISPLAY:
DESBIO
NDC 43742-1264-1
HOMEOPATHIC
BRONCHIAL COUGH
1 FL OZ (30 ml)
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 43742-1264 | BRONCHIAL COUGH (COCCUS CACTI, DROSERA (ROTUNDIFOLIA), SCILLA MARITIMA, STICTA PULMONARIA, CAUSTICUM, CUPRUM ACETICUM, ARSENICUM IODATUM, CARBO VEGETABILIS, KALI CARBONICUM, LACHESIS MUTUS) LIQUID [DESERET BIOLOGICALS, INC.] | 2 | Legacy NDC | 20210804_2eec96c0-1c80-4ce9-a421-9d3c18138e9d.zip |
Products#
Every source-derived product name is available through these pages.
- Bronchial Cough
- Coccus Cacti, Drosera (Rotundifolia), Scilla Maritima, Sticta Pulmonaria, Causticum, Cuprum Aceticum, Arsenicum Iodatum, Carbo Vegetabilis, Kali Carbonicum, Lachesis Mutus
- PROTORTONIA CACTI
- DROSERA ROTUNDIFOLIA
- DRIMIA MARITIMA BULB
- LOBARIA PULMONARIA
- CAUSTICUM
- CUPRIC ACETATE
- CUPRIC CATION
- ARSENIC TRIIODIDE
- ARSENIC CATION (3+)
- ACTIVATED CHARCOAL
- POTASSIUM CARBONATE
- CARBONATE ION
- LACHESIS MUTA VENOM
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43742-1264 | 43742-1264-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| PROTORTONIA CACTI | LZB7TFX1LT | ACTIB |
| DROSERA ROTUNDIFOLIA | QR44N9XPJQ | ACTIB |
| DRIMIA MARITIMA BULB | 3629601H5D | ACTIB |
| LOBARIA PULMONARIA | D1YM0P5Z2T | ACTIB |
| CAUSTICUM | DD5FO1WKFU | ACTIB |
| CUPRIC ACETATE | 39M11XPH03 | ACTIB |
| ARSENIC TRIIODIDE | 3029988O2T | ACTIB |
| ACTIVATED CHARCOAL | 2P3VWU3H10 | ACTIB |
| POTASSIUM CARBONATE | BQN1B9B9HA | ACTIB |
| LACHESIS MUTA VENOM | VSW71SS07I | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
Source Document#
openFDA label cross-check#
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 |
|---|---|---|---|---|---|---|
| 3f920c83-eb18-4827-9d6a-77a4360179c7 | 2eec96c0-1c80-4ce9-a421-9d3c18138e9d | 2021-08-03 | Warnings | 3f920c83-eb18-4827-9d6a-77a4360179c7 2eec96c0-1c80-4ce9-a421-9d3c18138e9d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.