Home NDC 44911-0592-1 Pulmopar
Product NDC 44911-0592
Requested package NDC 44911-0592-1
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 · 5 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…2024-05-28 21:12 UTC · source 2024-05-28 8af77b9d5b6f…d9bbb34c5368…2024-05-15 03:39 UTC · source 2024-05-14 834df4deac94…adcc014656a3…2024-03-11 06:39 UTC · source 2024-03-08 1332a3947898…d4bfe170f9cd…
Additional Listing Data#
Finished product Yes
Brand name base Pulmopar
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LOBELIA INFLATA WHOLE 12 [hp_X]/mL SUS SCROFA LUNG 12 [hp_X]/mL COMFREY ROOT 12 [hp_X]/mL ARSENIC TRIOXIDE 6 [hp_X]/mL BLATTA ORIENTALIS 3 [hp_X]/mL BRYONIA ALBA WHOLE 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL SULFUR 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 9 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0592-1 Pulmopar 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0592 PULMOPAR (LOBELIA INFLATA, LUNG (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BLATTA ORIENTALIS, BRYONIA (ALBA), PHOSPHORUS, SILICEA, SULPHUR) LIQUID [ENERGIQUE, INC.] 2 Current NDC, Legacy NDC, 1 package rows 20241031_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 Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Pulmopar LOBELIA INFLATA, LUNG (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BLATTA ORIENTALIS, BRYONIA (ALBA), PHOSPHORUS, SILICEA, SULPHUR Energique, Inc. 1cfb69c5-dc01-4acc-8053-5ca4e64165dc 2024-10-29 Warnings Exact identifier ndc (package): 44911-0592-1 ndc (product): 44911-0592 ndc11 (package): 44911059201
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0592-1 44911059201 30 mL in 1 BOTTLE, DROPPER (44911-0592-1) 30 ml 2021-05-27 0000-00-00 No No Current