Home FDA labels 58c571c8-1ee3-4fa3-ae53-63e65d8bd9a9 Dentastat 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 Dentastat
Generic name ALLIUM SATIVUM, BERBERIS VULGARIS, FUCUS VESICULOSUS, PHYTOLACCA DECANDRA, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, IODIUM, MERCURIUS SOLUBILIS, NICCOLUM METALLICUM, SILICEA, ZINCUM METALLICUM, PLATINUM METALLICUM
Manufacturer Energique, Inc.
Product type HUMAN OTC DRUG
SPL set ID 12786efd-df42-4321-bfdf-88f542d387bb
SPL ID 58c571c8-1ee3-4fa3-ae53-63e65d8bd9a9
Version 3
Effective date 2026-05-06
Source export date 2026-09-28
Source partition 11
Source file https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 06:18:17 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Dentastat openfda.brand_name generic name ALLIUM SATIVUM, BERBERIS VULGARIS, FUCUS VESICULOSUS, PHYTOLACCA DECANDRA, ARGENTUM METALLICUM, AURUM METALLICUM, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, HEKLA LAVA, HYDROFLUORICUM ACIDUM, IODIUM, MERCURIUS SOLUBILIS, NICCOLUM METALLICUM, SILICEA, ZINCUM METALLICUM, PLATINUM METALLICUM openfda.generic_name manufacturer name Energique, Inc. openfda.manufacturer_name ndc package 44911-0661-1 openfda.package_ndc ndc product 44911-0661 openfda.product_ndc ndc11 package 44911066101 derived:openfda.package_ndc spl id 58c571c8-1ee3-4fa3-ae53-63e65d8bd9a9 id spl set id 12786efd-df42-4321-bfdf-88f542d387bb set_id unii 3M4G523W1G openfda.unii unii V1V998DC17 openfda.unii unii 11E6VI8VEG openfda.unii unii O3B55K4YKI openfda.unii unii 324Y4038G2 openfda.unii unii 1TH8Q20J0U openfda.unii unii 91D9GV0Z28 openfda.unii unii 9679TC07X4 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii RGL5YE86CZ openfda.unii unii 79Y1949PYO openfda.unii unii C21158IIRK openfda.unii unii 535G2ABX9M openfda.unii unii 7OV03QG267 openfda.unii unii J41CSQ7QDS openfda.unii unii 49DFR088MY 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: Stop use and ask a doctor if symptoms persist for more than 7 days. 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.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.