Quantum Resonance

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: Quantum Resonance
Generic name: ALCOHOLUS, ALUMINA SILICATA, ANACARDIUM ORIENTALE, AQUA MARINA, BAPTISIA TINCTORIA, CANDIDA ALBICANS, COLLAGEN, DNA, LAVANDULA OFFICINALIS, MEDULLA OSSIS SUIS, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NUX MOSCHATA, PHOSPHORUS, QUARTZ, SILICEA, TELA ARANEA, VALERIANA OFFICINALIS, VISCUM ALBUM
Manufacturer: Deseret Biologicals, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f94a10bd-1c40-42c7-b458-b58070614549
SPL ID: bee482fb-048a-4da1-b712-3881869e174b
Version: 1
Effective date: 2026-04-10
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:55:56

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 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Quantum Resonance	openfda.brand_name
generic name		ALCOHOLUS, ALUMINA SILICATA, ANACARDIUM ORIENTALE, AQUA MARINA, BAPTISIA TINCTORIA, CANDIDA ALBICANS, COLLAGEN, DNA, LAVANDULA OFFICINALIS, MEDULLA OSSIS SUIS, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NUX MOSCHATA, PHOSPHORUS, QUARTZ, SILICEA, TELA ARANEA, VALERIANA OFFICINALIS, VISCUM ALBUM	openfda.generic_name
manufacturer name		Deseret Biologicals, Inc.	openfda.manufacturer_name
ndc	package	43742-2545-1	openfda.package_ndc
ndc	product	43742-2545	openfda.product_ndc
ndc11	package	43742254501	derived:openfda.package_ndc
spl id		bee482fb-048a-4da1-b712-3881869e174b	id
spl set id		f94a10bd-1c40-42c7-b458-b58070614549	set_id
unii		27YLU75U4W	openfda.unii
unii		6LK42KUV6W	openfda.unii
unii		51FI676N6F	openfda.unii
unii		VP2CN2G7Y8	openfda.unii
unii		AEE24M3MQ9	openfda.unii
unii		19AH1RAF4M	openfda.unii
unii		ETJ7Z6XBU4	openfda.unii
unii		4D7G21HDBC	openfda.unii
unii		451W47IQ8X	openfda.unii
unii		24H4NWX5CO	openfda.unii
unii		JWF5YAW3QW	openfda.unii
unii		BK9092J5MP	openfda.unii
unii		5EF0HWI5WU	openfda.unii
unii		Y0F0BU8RDU	openfda.unii
unii		3K9958V90M	openfda.unii
unii		FHJ3ATL51C	openfda.unii
unii		70WT22SF4B	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: If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: Sealed for your protection. Do not use if seal is broken or missing.

Reported adverse events (FAERS/openFDA)#

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