FDA.reportPublic FDA data

GBLV HP

Manufacturer
Natural Creations, Inc. | OHM Pharma, Inc.
Effective date
2025-12-12
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:35:46

Label at a glance#

ProductGBLV HP
Active ingredientATROPA BELLADONNA, BERBERIS VULGARIS ROOT BARK, MILK THISTLE, CHELIDONIUM MAJUS, CITRULLUS COLOCYNTHIS FRUIT PULP, DIOSCOREA VILLOSA TUBER, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, ANEMONE PULSATILLA, VERATRUM ALBUM ROOT
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*) - equal amounts of: Belladonna 30C, Berberis Vulg 30C, Carduus Mar 30C, Chelidonium Maj 30C, Colocynthis 30C, Dioscorea 30C, Hydrastis 30C, Lycopodium 30C, Nat Sulphuricum 30C, Nux Vom 30C, Phos 30C, Pulsatilla 30C, Veratrum Alb 30C.

OTC - PURPOSE SECTION

USES: Temporarily relieves flatulence, constipation, and belching.**

INDICATIONS & USAGE SECTION

USES: Temporarily relieves flatulence, constipation, and belching.**

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

WARNINGS SECTION

WARNINGS:

* Consult a physician for use in children under 12 years of age.

* IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.

* KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

* Do not use if TAMPER EVIDENT seal is broken or missing.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

OTC - QUESTIONS SECTION

QUESTIONS & COMMENTS?

Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

REFERENCES SECTION

* The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

** These statements have not been reviewed by the FDA. They are based on traditional homeopathic practice.

LOT: 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0613-1  

GBLV HP

Excess Bloating**

HOMEOPATHIC

1 fl oz (30 mL) / 20% Alcohol

GMP Logo UPC: 87773004499 NON GMO Logo

image descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130877730004499GTIN-13: 0877730004499
EAN-13: 0877730004499
GTIN-12: 877730004499
UPC-A: 877730004499
GTIN storage (14 digits): 00877730004499		GBLV HP.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
95250459-30e4-45c1-b08a-993044f49109Product name220250805
362d7abb-94e6-4c60-9a58-266894157713Product name120231023
9badc7be-250a-44ab-aa36-926af3f02679Product name120210527
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
26acd337-b838-40ac-bcbc-05c3b81c8712Product name120170323

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43406-0613-12022-03-03C16284748780-1d6a99b39-ba2e-a426-e053-dadaa90af4c2GBLV HP
43406-0613-12022-01-28C16284748780-1d6a99b39-ba2e-a426-e053-dadaa90af4c2GBLV HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43406-0613-1GBLV HP30 mL in 1 BOTTLE, DROPPERLIQUID305

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43406-061343406-0613-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATROPA BELLADONNAWQZ3G9PF0HACTIB
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
MILK THISTLEU946SH95EEACTIB
CHELIDONIUM MAJUS7E889U5RNNACTIB
CITRULLUS COLOCYNTHIS FRUIT PULP23H32AOH17ACTIB
DIOSCOREA VILLOSA TUBERIWY3IWX2G8ACTIB
GOLDENSEALZW3Z11D0JVACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
SODIUM SULFATE0YPR65R21JACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
PHOSPHORUS27YLU75U4WACTIB
ANEMONE PULSATILLAI76KB35JEVACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
GBLV HPATROPA BELLADONNA, BERBERIS VULGARIS ROOT BARK, MILK THISTLE, CHELIDONIUM MAJUS, CITRULLUS COLOCYNTHIS FRUIT PULP, DIOSCOREA VILLOSA TUBER, GOLDENSEAL, LYCOPODIUM CLAVATUM SPORE, SODIUM SULFATE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORUS, ANEMONE PULSATILLA, VERATRUM ALBUM ROOTNatural Creations, Inc.cff4d830-6696-4cde-9cd7-4ce55e28b54b2025-12-12WarningsExact identifier
ndc (package): 43406-0613-1
ndc (product): 43406-0613
ndc11 (package): 43406061301
spl id: 80fed459-9130-46b5-906d-b6d90be133ca
spl set id: cff4d830-6696-4cde-9cd7-4ce55e28b54b

Reported adverse events (FAERS/openFDA)#

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