GI Clear P

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2025-05-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:33:34

Label at a glance#

ProductGI Clear P
Active ingredientARSENIC TRIOXIDE, BAPTISIA TINCTORIA ROOT, LACHESIS MUTA VENOM, PULSATILLA PRATENSIS WHOLE, TOXICODENDRON PUBESCENS LEAF
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 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): 20% of Arsenicum Album 10X, Baptisia Tinctoria 10X, Lachesis Mutus 10X, Pulsatilla (Pratensis) 10X, Rhus Tox 10X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve nausea, diarrhea, abdominal cramping, gas, bloatin, dehydration, and fever.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health 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 a 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 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 2 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 nausea, diarrhea, abdominal cramping, gas, bloatin, dehydration, and fever.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% 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

GI CLEAR P

2 fl. oz. (60 ml)

GI Clear PGI Clear P

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
44911-0611-12023-11-17C16284748780-1f386c64a-1d4a-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0611-12023-01-30C16284748780-1f386c64a-1d4a-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0611-1GI Clear P60 mL in 1 BOTTLE, DROPPERLIQUID603

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0611GI CLEAR P (ARSENICUM ALBUM, BAPTISIA TINCTORIA, LACHESIS MUTUS, PULSATILLA (PRATENSIS), RHUS TOX) LIQUID [ENERGIQUE, INC.]3Current NDC, Legacy NDC, 1 package rows20250519_9aca850f-7e18-4147-aaf1-f6f04047f7f3.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-061144911-0611-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
GI Clear PARSENICUM ALBUM, BAPTISIA TINCTORIA, LACHESIS MUTUS, PULSATILLA (PRATENSIS), RHUS TOXEnergique, Inc.9aca850f-7e18-4147-aaf1-f6f04047f7f32025-05-16WarningsExact identifier
ndc (package): 44911-0611-1
ndc (product): 44911-0611
ndc11 (package): 44911061101
spl id: 787bc0d6-e847-4983-b9eb-e1bbba4c7c9c
spl set id: 9aca850f-7e18-4147-aaf1-f6f04047f7f3

Reported adverse events (FAERS/openFDA)#

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