Gastropar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:23

Label at a glance#

ProductGastropar
Active ingredientGENTIANA 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
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(in each drop): 12.48% of Arsenicum Album 12X, Bismuthum Subnitricum 12X, Carbo Vegetabilis 12X, Lycopodium Clavatum 12X, Nux Vomica 12X, Phosphorus 12X, Stomach (Suis) 6X, Symphytum Officinale 6X; 0.10% of Gentiana Lutea 3X, Sambucus Nigra 3X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve indigestion, flatulence, nausea, retching, vomiting after eating or drinking, and minor burning in the stomach.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

Adults and children 5 to 10 orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

INDICATIONS & USAGE SECTION

May temporarily relieve indigestion, flatulence, nausea, retching, vomiting after eating or drinking, and minor burning in the stomach.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 25% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

Dist. by Energique, Inc.
201 Apple Blvd
Woodbine, IA 51579   800.869.8078

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

GASTROPAR

1 fl. oz. (30 ml)

GastroparGastropar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
63f39a63-5cd1-4016-bd86-2bbb0f6c3139Product name320240506
e5a77e9c-c528-733a-173d-914a234c024bProduct name520240506
0be8e4ae-4d57-49f3-b3a9-e4728b4e8d15Product name120240313
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0425-12024-10-24C16284748780-1ba0f9c33-3c45-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0425-12023-01-30C16284748780-1ba0f9c33-3c45-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0425-12021-08-02C16284748780-1ba0f9c33-3c45-a910-e053-dadaa90a0b85DRUG FACTS:
44911-0425-12021-01-29C16284748780-1ba0f9c33-3c45-a910-e053-dadaa90a0b85DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0425-1Gastropar30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0425GASTROPAR (GENTIANA LUTEA, SAMBUCUS NIGRA, STOMACH (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BISMUTHUM SUBNITRICUM, CARBO VEGETABILIS, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUS) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241027_128b917d-2d92-4c41-bbc4-09f916b822a5.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-042544911-0425-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

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
GastroparGENTIANA LUTEA, SAMBUCUS NIGRA, STOMACH (SUIS), SYMPHYTUM OFFICINALE, ARSENICUM ALBUM, BISMUTHUM SUBNITRICUM, CARBO VEGETABILIS, LYCOPODIUM CLAVATUM, NUX VOMICA, PHOSPHORUSEnergique, Inc.128b917d-2d92-4c41-bbc4-09f916b822a52024-10-24WarningsExact identifier
ndc (package): 44911-0425-1
ndc (product): 44911-0425
ndc11 (package): 44911042501
spl id: 47e8134f-0d3c-4dfc-9003-2d0f0565aea8
spl set id: 128b917d-2d92-4c41-bbc4-09f916b822a5

Reported adverse events (FAERS/openFDA)#

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