Pneumopar

Product NDC: 44911-0374
Requested package NDC: 44911-0374-1
11-digit product format: 449110374
Labeler code: 44911
Product ID: 44911-0374_b0282e4a-7670-4a1a-a687-938a1f8baf9d
Type: HUMAN OTC DRUG
Nonproprietary name: Lobelia Inflata, Lung (Suis), Symphytum Officinale, Arsenicum Album, Blatta Orientalis, Bryonia (Alba), Phosphorus, Silicea, Sulphur
Dosage form: LIQUID
Route: ORAL
Labeler: Energique, Inc.
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2016-07-26
Marketing end: 2025-03-24
Substance: ARSENIC TRIOXIDE; BLATTA ORIENTALIS; BRYONIA ALBA ROOT; COMFREY ROOT; LOBELIA INFLATA; PHOSPHORUS; SILICON DIOXIDE; SULFUR; SUS SCROFA LUNG
Active strength: 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes: Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Insect Allergenic Extract [EPC]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	44911-0374	44911-0374-1	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	44911-0374	44911-0374-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	44911-0374	44911-0374-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0374-1	2022-03-23	C162847	48780-1	d6a99b39-3922-a426-e053-dadaa90af4c2	Drug Facts:
44911-0374-1	2022-01-28	C162847	48780-1	d6a99b39-3922-a426-e053-dadaa90af4c2	Drug Facts:

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
S7V92P67HO	ARSENIC TRIOXIDE	1327-53-3	ARSENIC TRIOXIDE
535787266D	BLATTA ORIENTALIS		BLATTA ORIENTALIS
T7J046YI2B	BRYONIA ALBA ROOT		BRYONIA ALBA ROOT
M9VVZ08EKQ	COMFREY ROOT		COMFREY ROOT
9PP1T3TC5U	LOBELIA INFLATA		LOBELIA INFLATA
27YLU75U4W	PHOSPHORUS	7723-14-0	PHOSPHORUS
ETJ7Z6XBU4	SILICON DIOXIDE	7631-86-9	SILICON DIOXIDE
70FD1KFU70	SULFUR	7704-34-9	SULFUR
7GL3G1COB3	SUS SCROFA LUNG		SUS SCROFA LUNG

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
44911-0374-1	44911037401	30 mL in 1 BOTTLE, DROPPER (44911-0374-1)	30 ml	2016-07-26	2025-03-24	No	No	Current

Pneumopar

NDC auxiliary status#

Observed NDC auxiliary status history#

Reported adverse events (FAERS/openFDA)#

FDA-Initiated Inactive NDC Indexing#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#