Home NDC 44911-0425-1 Gastropar
Product NDC 44911-0425
Requested package NDC 44911-0425-1
11-digit product format 449110425
Labeler code 44911
Product ID 44911-0425_47e8134f-0d3c-4dfc-9003-2d0f0565aea8
Type HUMAN OTC DRUG
Nonproprietary name Gentiana Lutea, Sambucus Nigra, Stomach (Suis), Symphytum Officinale, Arsenicum Album, Bismuthum Subnitricum, Carbo Vegetabilis, Lycopodium Clavatum, Nux Vomica, Phosphorus
Dosage form LIQUID
Route ORAL
Labeler Energique, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2017-05-30
Substance GENTIANA LUTEA ROOT; SAMBUCUS NIGRA FLOWERING TOP; SUS SCROFA STOMACH; COMFREY ROOT; ARSENIC TRIOXIDE; BISMUTH SUBNITRATE; ACTIVATED CHARCOAL; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORUS
Active strength 3; 3; 6; 6; 12; 12; 12; 12; 12; 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; [hp_X]/mL
Pharmacologic classes Allergens [CS], Bismuth [CS], Bismuth [EPC], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]
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…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Gastropar
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength GENTIANA LUTEA ROOT 3 [hp_X]/mL SAMBUCUS NIGRA FLOWERING TOP 3 [hp_X]/mL SUS SCROFA STOMACH 6 [hp_X]/mL COMFREY ROOT 6 [hp_X]/mL ARSENIC TRIOXIDE 12 [hp_X]/mL BISMUTH SUBNITRATE 12 [hp_X]/mL ACTIVATED CHARCOAL 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 10 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 44911-0425-1 Gastropar 30 mL in 1 BOTTLE, DROPPER LIQUID 30 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0425 GASTROPAR (GENTIANA LUTEA, SAMBUCUS NIGRA, STOMACH (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BISMUTHUM SUBNITRICUM, CARBO VEGETABILIS, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUS) LIQUID [ENERGIQUE, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20241027_128b917d-2d92-4c41-bbc4-09f916b822a5.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 Gastropar GENTIANA LUTEA, SAMBUCUS NIGRA, STOMACH (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BISMUTHUM SUBNITRICUM, CARBO VEGETABILIS, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUS Energique, Inc. 128b917d-2d92-4c41-bbc4-09f916b822a5 2024-10-24 Warnings Exact identifier ndc (package): 44911-0425-1 ndc (product): 44911-0425 ndc11 (package): 44911042501
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 44911-0425-1 44911042501 30 mL in 1 BOTTLE, DROPPER (44911-0425-1) 30 ml 2017-05-30 0000-00-00 No No Current