Diabase

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: Diabase
Generic name: CYNARA, ECHINACEA, IRIS VERS., THUJA OCC., URTICA UR., ARG. MET., ARSENICUM ALB., AUR. MET., BOVISTA, BRYONIA, CHELIDONIUM MAJ., CHIONANTHUS, GAULTHERIA, HELONIAS, IRIS VERS., LYCOPODIUM, NUX VOM., PHOS., RHUS TOX., SABAL, SYZYGIUM
Manufacturer: Newton Laboratories, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 9948bd7a-2ca2-272c-e053-2a95a90a4dc0
SPL ID: b5827c57-cec4-947e-e053-2995a90ad297
Version: 2
Effective date: 2020-12-02
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:40:16

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Diabase	openfda.brand_name
generic name		CYNARA, ECHINACEA, IRIS VERS., THUJA OCC., URTICA UR., ARG. MET., ARSENICUM ALB., AUR. MET., BOVISTA, BRYONIA, CHELIDONIUM MAJ., CHIONANTHUS, GAULTHERIA, HELONIAS, IRIS VERS., LYCOPODIUM, NUX VOM., PHOS., RHUS TOX., SABAL, SYZYGIUM	openfda.generic_name
manufacturer name		Newton Laboratories, Inc.	openfda.manufacturer_name
ndc	package	55714-4751-1	openfda.package_ndc
ndc	product	55714-4751	openfda.product_ndc
ndc11	package	55714475101	derived:openfda.package_ndc
spl id		b5827c57-cec4-947e-e053-2995a90ad297	id
spl set id		9948bd7a-2ca2-272c-e053-2a95a90a4dc0	set_id
unii		27YLU75U4W	openfda.unii
unii		K2A74U428F	openfda.unii
unii		3M4G523W1G	openfda.unii
unii		820LSF646I	openfda.unii
unii		7E889U5RNN	openfda.unii
unii		J7WWH9M8QS	openfda.unii
unii		269XH13919	openfda.unii
unii		1NT28V9397	openfda.unii
unii		IHN2NQ5OF9	openfda.unii
unii		79Y1949PYO	openfda.unii
unii		6IO182RP7A	openfda.unii
unii		S7V92P67HO	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		T7J046YI2B	openfda.unii
unii		830295X963	openfda.unii
unii		X43D4L3DQC	openfda.unii
unii		DQV54Y5H3U	openfda.unii
unii		B71UA545DE	openfda.unii
unii		C88X29Y479	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 SECTION WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding , ask a doctor before use.

Reported adverse events (FAERS/openFDA)#

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