Pertussinum (nosode)

Manufacturer: Newton Laboratories, Inc.
Effective date: 2020-12-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 23:01:26

Label at a glance#

ProductPertussinum (nosode)

Active ingredientHUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1.800.448.7256

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Law of similars; Spasmatic coughing attacks

DOSAGE & ADMINISTRATION SECTION

Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) as needed or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.

OTC - ACTIVE INGREDIENT SECTION

Pertussinum 200c, Pertussinum 30c

OTC - PURPOSE SECTION

Law of similars; Spasmatic coughing attacks

INACTIVE INGREDIENT SECTION

Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.

QUESTIONS SECTION

OTC - QUESTIONS SECTION

newtonlabs.net - Questions? 1.800.448.7256

Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013

WARNINGS SECTION

WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Pertussinum (nosode)
WATER
ALCOHOL
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-6495	55714-6495-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	IACT
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	U364V64HUN	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0ccb8be1-48b4-b6ee-e063-6294a90a6a10			d96b1473-5cfb-bc9e-411b-92ecd6325b37	2023-12-18	Warnings	Exact identifier spl set id: d96b1473-5cfb-bc9e-411b-92ecd6325b37

Reported adverse events (FAERS/openFDA)#

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