Pulmopar

Product NDC
44911-0592
11-digit product format
449110592
Labeler code
44911
Product ID
44911-0592_651bc3c9-e713-400f-ac9b-4ca3fd23d8a6
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
2021-05-27
Substance
ARSENIC TRIOXIDE; BLATTA ORIENTALIS; BRYONIA ALBA WHOLE; COMFREY ROOT; LOBELIA INFLATA WHOLE; PHOSPHORUS; SILICON DIOXIDE; SULFUR; SUS SCROFA LUNG
Active strength
12; 12; 12; 6; 3; 12; 12; 12; 6 [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
2026-12-31
Current FDA listing
Yes

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 · 10 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2024-10-04 04:10 UTC · source 2024-10-03excluded productproduct367a005e9d99…383a685ebd0f…
2024-10-04 04:10 UTC · source 2024-10-03excluded packagepackage44911-0592-1367a005e9d99…383a685ebd0f…
2024-07-10 04:00 UTC · source 2024-07-09excluded productproduct557ba5c1ecfa…9c80585c8c6e…
2024-07-10 04:00 UTC · source 2024-07-09excluded packagepackage44911-0592-1557ba5c1ecfa…9c80585c8c6e…
2024-05-28 21:12 UTC · source 2024-05-28excluded productproduct8af77b9d5b6f…d9bbb34c5368…
2024-05-28 21:12 UTC · source 2024-05-28excluded packagepackage44911-0592-18af77b9d5b6f…d9bbb34c5368…
2024-05-15 03:39 UTC · source 2024-05-14excluded productproduct834df4deac94…adcc014656a3…
2024-05-15 03:39 UTC · source 2024-05-14excluded packagepackage44911-0592-1834df4deac94…adcc014656a3…
2024-03-11 06:39 UTC · source 2024-03-08excluded productproduct1332a3947898…d4bfe170f9cd…
2024-03-11 06:39 UTC · source 2024-03-08excluded packagepackage44911-0592-11332a3947898…d4bfe170f9cd…

Additional Listing Data#

Finished product
Yes
Brand name base
Pulmopar
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
LOBELIA INFLATA WHOLE12 [hp_X]/mL
SUS SCROFA LUNG12 [hp_X]/mL
COMFREY ROOT12 [hp_X]/mL
ARSENIC TRIOXIDE6 [hp_X]/mL
BLATTA ORIENTALIS3 [hp_X]/mL
BRYONIA ALBA WHOLE12 [hp_X]/mL
PHOSPHORUS12 [hp_X]/mL
SILICON DIOXIDE12 [hp_X]/mL
SULFUR6 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 9 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
9PP1T3TC5UInternal UNII lookup
7GL3G1COB3Internal UNII lookup
M9VVZ08EKQInternal UNII lookup
S7V92P67HOInternal UNII lookup
535787266DInternal UNII lookup
56K0VVT47PInternal UNII lookup
27YLU75U4WInternal UNII lookup
ETJ7Z6XBU4Internal UNII lookup
70FD1KFU70Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1cfb69c5-dc01-4acc-8053-5ca4e64165dcAvailable on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0592-12024-10-29C16284748780-1f386c649-d179-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0592-12023-01-30C16284748780-1f386c649-d179-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0592-1Pulmopar30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0592PULMOPAR (LOBELIA INFLATA, LUNG (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BLATTA ORIENTALIS, BRYONIA (ALBA), PHOSPHORUS, SILICEA, SULPHUR) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241031_1cfb69c5-dc01-4acc-8053-5ca4e64165dc.zip

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
PulmoparLOBELIA INFLATA, LUNG (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BLATTA ORIENTALIS, BRYONIA (ALBA), PHOSPHORUS, SILICEA, SULPHUREnergique, Inc.1cfb69c5-dc01-4acc-8053-5ca4e64165dc2024-10-29WarningsExact identifier
ndc (product): 44911-0592

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
44911-0592-14491105920130 mL in 1 BOTTLE, DROPPER (44911-0592-1) 30 ml2021-05-270000-00-00NoNoCurrent