Pertussinum

Manufacturer: Newton Laboratories, Inc.
Effective date: 2023-11-13
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 02:24:03

Label at a glance#

ProductPertussinum

Active ingredientHUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED

Label structure10 sections

Contacts and useful links#

PhoneLabel contact800.448.7256

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Law of similars; Spasmatic coughing attacks

DOSAGE & ADMINISTRATION SECTION

Directions: 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 (nosode) 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? 800.448.7256

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

WARNINGS SECTION

Warning: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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55714-9011-1	2023-11-13	C162847	48780-1	d6a99b39-5291-a426-e053-dadaa90af4c2	Pertussinum 9011L
55714-9011-1	2022-01-28	C162847	48780-1	d6a99b39-5291-a426-e053-dadaa90af4c2	Pertussinum 9011L

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
55714-9011-1	Pertussinum	30 mL in 1 BOTTLE, GLASS	LIQUID	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
55714-9011	PERTUSSINUM LIQUID [NEWTON LABORATORIES, INC.]	2	Legacy NDC, 1 package rows	20231114_9e3c2059-4e58-54b2-e053-2a95a90a24f6.zip

Products#

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

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

Pertussinum
ALCOHOL
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55714-9011	55714-9011-1

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
ALCOHOL	3K9958V90M	IACT
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	U364V64HUN	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML · Source PDF

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
53483c87-54b8-edd1-e063-6294a90ad5c4			9e3c2059-4e58-54b2-e053-2a95a90a24f6	2026-06-02	Warnings	Exact identifier spl set id: 9e3c2059-4e58-54b2-e053-2a95a90a24f6

Reported adverse events (FAERS/openFDA)#

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