FDA.reportPublic FDA data

Pertussis

Manufacturer
Deseret Biologicals, Inc. | Apotheca Company
Effective date
2022-02-15
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:08:37

Label at a glance#

ProductPertussis
Active ingredientIPECAC, LOBARIA PULMONARIA, PHOSPHORUS, ANTIMONY POTASSIUM TARTRATE, WOOD CREOSOTE, ACONITUM NAPELLUS, BRYONIA ALBA ROOT, HYOSCYAMUS NIGER, SILICON DIOXIDE, TOBACCO LEAF, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, CLOSTRIDIUM TETANI
Label structure9 sections

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

Ipecacuanha 4X, Sticta Pulmonaria 4X, Phosphorus 5X, Antimonium Tartaricum 6X, Kreosotum 6X, Aconitum Napellus 8X, Bryonia (Alba) 8X, Hyoscyamus Niger 8X, Silicea 8X, Tabacum 8X, Pertussinum 30X, Tetanus Toxin 30X.

HOMEOPATHIC INDICATIONS:

OTC - PURPOSE SECTION

For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, and vaccination
reactions.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INDICATIONS & USAGE SECTION

For temporary relief of symptoms related to Pertussis infection including cough, bronchial congestion, fever, and vaccination
reactions.**

**These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized Water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. By: Deseret Biologicals, Inc.
469 W. Parkland Drive
Sandy, UT 84070 www.desbio.com

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DESBIO
NDC 43742-1320-1
HOMEOPATHIC
PERTUSSIS
1 FL OZ (30 ml)

PertussisPertussis

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43742-1320-12022-02-15C16284748780-1d6a99b39-b9cb-a426-e053-dadaa90af4c2Drug Facts:
43742-1320-12022-01-28C16284748780-1d6a99b39-b9cb-a426-e053-dadaa90af4c2Drug Facts:

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43742-132043742-1320-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
NameUNIIKind
IPECAC62I3C8233LACTIB
LOBARIA PULMONARIAD1YM0P5Z2TACTIB
PHOSPHORUS27YLU75U4WACTIB
ANTIMONY POTASSIUM TARTRATEDL6OZ476V3ACTIB
WOOD CREOSOTE3JYG22FD73ACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
BRYONIA ALBA ROOTT7J046YI2BACTIB
HYOSCYAMUS NIGER4WRK2153H3ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
TOBACCO LEAF6YR2608RSUACTIB
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTEDU364V64HUNACTIB
CLOSTRIDIUM TETANI751E8J54VMACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
1ab03905-9088-4cfe-bac8-b57ce2c821631b0b85ef-1fcc-461d-876f-315786eaa7472022-02-15WarningsExact identifier
spl id: 1ab03905-9088-4cfe-bac8-b57ce2c82163
spl set id: 1b0b85ef-1fcc-461d-876f-315786eaa747

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.