Home NDC 43742-2545 Quantum Resonance
Product NDC 43742-2545
11-digit product format 437422545
Labeler code 43742
Product ID 43742-2545_bee482fb-048a-4da1-b712-3881869e174b
Type HUMAN OTC DRUG
Nonproprietary 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
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-04-10
Substance ALCOHOL; KAOLIN; SEMECARPUS ANACARDIUM JUICE; SODIUM CHLORIDE; BAPTISIA TINCTORIA ROOT; CANDIDA ALBICANS; BOVINE TYPE I COLLAGEN; HERRING SPERM DNA; LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER; SUS SCROFA BONE MARROW; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; NUTMEG; PHOSPHORUS; SILICON DIOXIDE; BOMBYX MORI FIBER; VALERIAN; VISCUM ALBUM FRUITING TOP
Active strength 30; 30; 30; 6; 30; 30; 6; 15; 6; 8; 6; 30; 12; 12; 200; 30; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_Q]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Allergens [CS], Allergens [CS], Allogeneic Cultured Cell Scaffold [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Collagen [CS], Dietary Proteins [CS], Food Additives [CS], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Insect Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Insect Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Silk [CS]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Quantum Resonance
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ALCOHOL 30 [hp_X]/mL KAOLIN 30 [hp_X]/mL SEMECARPUS ANACARDIUM JUICE 30 [hp_X]/mL SODIUM CHLORIDE 6 [hp_X]/mL BAPTISIA TINCTORIA ROOT 30 [hp_X]/mL CANDIDA ALBICANS 30 [hp_X]/mL BOVINE TYPE I COLLAGEN 6 [hp_X]/mL HERRING SPERM DNA 15 [hp_X]/mL LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER 6 [hp_Q]/mL SUS SCROFA BONE MARROW 8 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 6 [hp_X]/mL NUTMEG 30 [hp_X]/mL PHOSPHORUS 12 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL BOMBYX MORI FIBER 200 [hp_X]/mL VALERIAN 30 [hp_X]/mL VISCUM ALBUM FRUITING TOP 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 17 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2545-1 Quantum Resonance 30 mL in 1 BOTTLE, DROPPER LIQUID 30 1
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Quantum Resonance 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 Deseret Biologicals, Inc. f94a10bd-1c40-42c7-b458-b58070614549 2026-04-10 Warnings Exact identifier ndc (product): 43742-2545
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43742-2545-1 43742254501 30 mL in 1 BOTTLE, DROPPER (43742-2545-1) 30 ml 2026-04-10 No No Current