Home DailyMed 214eb19a-e7a2-421c-9f34-724ce430185c DRUG FACTS: Drug label information. FDA.report displays public Structured Product Labeling data from DailyMed and legacy FDA.report DailyMed cache rows. This page is not medical advice, prescribing advice, or a substitute for the official label reviewed by a qualified healthcare professional. Labeling can change; when a current hydrated DailyMed SPL record is available, FDA.report shows that newer record before legacy cached files.
Manufacturer Deseret Biologicals, Inc. | Apotheca Company
Effective date 2026-04-10
Label type HUMAN OTC DRUG LABEL
Version 2
Source full-release
Hydrated at 2026-06-01 02:38:19 Label at a glance# Product Connection
Active ingredient SEMECARPUS ANACARDIUM JUICE, SODIUM TETRACHLOROAURATE, CAMPHOR (NATURAL), HERRING SPERM DNA, GERMANIUM, HELLEBORUS NIGER ROOT, HYDROGEN, CANIS LUPUS FAMILIARIS MILK, HUMAN MILK, LITHIUM CARBONATE, MAGNESIUM OXIDE, SODIUM CARBONATE, NEON, OXYTOCIN, SUS SCROFA PLACENTA, RHUS GLABRA TOP, SUCROSE, DATURA STRAMONIUM, THUJA OCCIDENTALIS LEAFY TWIG
Label structure 9 sections
Indications and uses • For the temporary relief of symptoms including: • desire for intimacy • forsaken feeling • isolation • disconnection • alienation • lack of mother child bonding • loneliness • estrangement • feeling unloved These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Dosage and administration 1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
Product Linked Resources# DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-2356-1 Connection 30 mL in 1 BOTTLE, DROPPER LIQUID 30 2
Products# Every source-derived product name is available through these pages.
DailyMed product names page 1 of 1 · 27 matching rows.
Connection Anacardium Orientale, Aurum Muriaticum Natronatum, Camphora, DNA, Germanium Metallicum, Helleborus Niger, Hydrogen, Lac Caninum, Lac Materna Humanum, Lithium Carbonicum, Lithium Carbonicum, Magnesia Oxydata, Natrum Carbonicum, Neon, Oxytocin, Placenta Totalis Suis, Rhus Glabra, Saccharum Officinale, Stramonium, Thuja Occidentalis SEMECARPUS ANACARDIUM JUICE SODIUM TETRACHLOROAURATE TETRACHLOROAURATE ION CAMPHOR (NATURAL) HERRING SPERM DNA GERMANIUM HELLEBORUS NIGER ROOT HYDROGEN CANIS LUPUS FAMILIARIS MILK HUMAN MILK LITHIUM CARBONATE LITHIUM CATION MAGNESIUM OXIDE MAGNESIUM CATION SODIUM CARBONATE CARBONATE ION NEON OXYTOCIN SUS SCROFA PLACENTA RHUS GLABRA TOP SUCROSE DATURA STRAMONIUM THUJA OCCIDENTALIS LEAFY TWIG WATER ALCOHOL Ingredients# Every source-derived ingredient row is available through these pages.
DailyMed ingredient rows page 1 of 1 · 21 matching rows.
Older Hydrated Versions# Version, Effective date, Source table Version Effective date Source Hydrated 1 2026-02-19 monthly-update 2026-06-03 17:55:58
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 Connection ANACARDIUM ORIENTALE, AURUM MURIATICUM NATRONATUM, CAMPHORA, DNA, GERMANIUM METALLICUM, HELLEBORUS NIGER, HYDROGEN, LAC CANINUM, LAC MATERNA HUMANUM, LITHIUM CARBONICUM, LITHIUM CARBONICUM, MAGNESIA OXYDATA, NATRUM CARBONICUM, NEON, OXYTOCIN, PLACENTA TOTALIS SUIS, RHUS GLABRA, SACCHARUM OFFICINALE, STRAMONIUM, THUJA OCCIDENTALIS Deseret Biologicals, Inc. 214eb19a-e7a2-421c-9f34-724ce430185c 2026-04-10 Warnings Exact identifier ndc (package): 43742-2356-1 ndc (product): 43742-2356 ndc11 (package): 43742235601 spl id: f6beea73-ec85-4b1b-8dcb-88ff69530137 spl set id: 214eb19a-e7a2-421c-9f34-724ce430185c
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.