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, PALLADIUM METALLICUM, PHOSPHORUS, SILICEA, TITANIUM METALLICUM, ZINCUM METALLICUM, PLATINUM METALLICUM, PYROGENIUM
Manufacturer: Energique, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 7f6d360b-9fee-4374-a47c-847806d54fa0
SPL ID: 5ca78b9d-18a0-4cd9-b48d-73dd15b4d1be
Version: 1
Effective date: 2026-04-13
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:48:06

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 · 28 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, PALLADIUM METALLICUM, PHOSPHORUS, SILICEA, TITANIUM METALLICUM, ZINCUM METALLICUM, PLATINUM METALLICUM, PYROGENIUM	openfda.generic_name
manufacturer name		Energique, Inc.	openfda.manufacturer_name
ndc	package	44911-0906-1	openfda.package_ndc
ndc	product	44911-0906	openfda.product_ndc
ndc11	package	44911090601	derived:openfda.package_ndc
spl id		5ca78b9d-18a0-4cd9-b48d-73dd15b4d1be	id
spl set id		7f6d360b-9fee-4374-a47c-847806d54fa0	set_id
unii		27YLU75U4W	openfda.unii
unii		3M4G523W1G	openfda.unii
unii		5TWQ1V240M	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		29SUH5R3HU	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		D1JT611TNE	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.