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.
Pertussis
- Manufacturer
- Deseret Biologicals, Inc. | Apotheca Company
- Effective date
- 2018-04-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:59:23
Label at a glance#
ProductPertussis
Active ingredientACONITUM NAPELLUS, ATROPA BELLADONNA, BRYONIA ALBA ROOT, HYOSCYAMUS NIGER, IPECAC, LOBARIA PULMONARIA, TOBACCO LEAF, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, WOOD CREOSOTE, SILICON DIOXIDE, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, CLOSTRIDIUM TETANI
Label structure9 sections
Contacts and useful links#
Websitewww.desbio.com
www.desbio.com
www.desbio.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
Aconitum Napellus 4X, Belladonna 4X, Bryonia (Alba) 4X, Hyoscyamus Niger 4X, Ipecacuanha 4X, Sticta Pulmonaria 4X, Tabacum 4X, Phosphorus 5X, Antimonium Tartaricum 6X, Kreosotum 6X, Silicea 8X, Pertussinum 30X, Tetanus Toxin 30X.
HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, whooping cough and vaccination reactions.**
**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 Pertussis infection including cough, bronchial congestion, fever, whooping cough and vaccination reactions.**
**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:
PACKAGE LABEL DISPLAY:
DESBIO
NDC 43742-0916-1
HOMEOPATHIC
PERTUSSIS
1 FL OZ (30 ml)
Products#
Every source-derived product name is available through these pages.
- Pertussis
- Aconitum Napellus, Belladonna, Bryonia (Alba), Hyoscyamus Niger, Ipecacuanha, Sticta Pulmonaria, Tabacum, Phosphorus, Antimonium Tartaricum, Kreosotum, Silicea, Pertussinum, Tetanus Toxin
- ACONITUM NAPELLUS
- ATROPA BELLADONNA
- BRYONIA ALBA ROOT
- HYOSCYAMUS NIGER
- IPECAC
- LOBARIA PULMONARIA
- TOBACCO LEAF
- PHOSPHORUS
- ANTIMONY POTASSIUM TARTRATE
- ANTIMONY CATION (3+)
- WOOD CREOSOTE
- SILICON DIOXIDE
- HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
- CLOSTRIDIUM TETANI
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43742-0916 | 43742-0916-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACONITUM NAPELLUS | U0NQ8555JD | ACTIB |
| ATROPA BELLADONNA | WQZ3G9PF0H | ACTIB |
| BRYONIA ALBA ROOT | T7J046YI2B | ACTIB |
| HYOSCYAMUS NIGER | 4WRK2153H3 | ACTIB |
| IPECAC | 62I3C8233L | ACTIB |
| LOBARIA PULMONARIA | D1YM0P5Z2T | ACTIB |
| TOBACCO LEAF | 6YR2608RSU | ACTIB |
| PHOSPHORUS | 27YLU75U4W | ACTIB |
| ANTIMONY POTASSIUM TARTRATE | DL6OZ476V3 | ACTIB |
| WOOD CREOSOTE | 3JYG22FD73 | ACTIB |
| SILICON DIOXIDE | ETJ7Z6XBU4 | ACTIB |
| HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED | U364V64HUN | ACTIB |
| CLOSTRIDIUM TETANI | 751E8J54VM | 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 |
|---|---|---|---|---|---|---|
| 0fb85851-8de2-480d-b3c9-cbef68e915bf | 23db9296-b4f8-4b62-9daa-c8e696ed86ad | 2018-04-25 | Warnings | 0fb85851-8de2-480d-b3c9-cbef68e915bf 23db9296-b4f8-4b62-9daa-c8e696ed86ad |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.