Home FDA labels 80fed459-9130-46b5-906d-b6d90be133ca GBLV HP openFDA label record# This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)
Brand name GBLV HP
Generic name ATROPA 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
Manufacturer Natural Creations, Inc.
Product type HUMAN OTC DRUG
SPL set ID cff4d830-6696-4cde-9cd7-4ce55e28b54b
SPL ID 80fed459-9130-46b5-906d-b6d90be133ca
Version 5
Effective date 2025-12-12
Source export date 2026-09-28
Source partition 10
Source file https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:07:37 Harmonized routes table Harmonized routes ORAL
Harmonized identifier links# Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Harmonized identifiers page 1 of 1 · 21 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name GBLV HP openfda.brand_name generic name ATROPA 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 openfda.generic_name manufacturer name Natural Creations, Inc. openfda.manufacturer_name ndc package 43406-0613-1 openfda.package_ndc ndc product 43406-0613 openfda.product_ndc ndc11 package 43406061301 derived:openfda.package_ndc spl id 80fed459-9130-46b5-906d-b6d90be133ca id spl set id cff4d830-6696-4cde-9cd7-4ce55e28b54b set_id unii 27YLU75U4W openfda.unii unii IWY3IWX2G8 openfda.unii unii 7E889U5RNN openfda.unii unii 269XH13919 openfda.unii unii 0YPR65R21J openfda.unii unii 1TH8Q20J0U openfda.unii unii U946SH95EE openfda.unii unii ZW3Z11D0JV openfda.unii unii WQZ3G9PF0H openfda.unii unii I76KB35JEV openfda.unii unii QNS6W5US1Z openfda.unii unii C88X29Y479 openfda.unii unii 23H32AOH17 openfda.unii
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Warnings sections page 1 of 1 · 1 matching rows.
warnings 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.